Linked Data
dbSNP Id:
rs377717467
ExAC:
19:41198163 G / A
gnomAD v2:
19-41198163-G-A
gnomAD v3:
19-40692258-G-A
gnomAD v4:
19-40692258-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40692258G>A , CM000681.2:g.40692258G>A | GRCh38 |
| NC_000019.9:g.41198163G>A , CM000681.1:g.41198163G>A | GRCh37 |
| NC_000019.8:g.45890003G>A | NCBI36 |
| NG_027800.1:g.29628C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324464.8:c.1412C>T MANE Select | ENSP00000315118.3:p.Pro471Leu | |
| ENST00000593724.2:n.3235C>T | ||
| ENST00000594490.6:c.1334C>T | ENSP00000471310.2:p.Pro445Leu | |
| ENST00000594720.6:c.1412C>T | ENSP00000470876.2:p.Pro471Leu | |
| ENST00000596455.6:n.1704C>T | ||
| ENST00000601967.6:c.1412C>T | ENSP00000470916.2:p.Pro471Leu | |
| ENST00000676555.1:c.*837C>T | ENSP00000503387.1:n.*837C>T | |
| ENST00000676578.1:c.*1154C>T | ENSP00000504076.1:n.*1154C>T | |
| ENST00000676960.1:n.1537C>T | ||
| ENST00000676962.1:n.1691C>T | ||
| ENST00000677018.1:c.1412C>T | ENSP00000503480.1:p.Pro471Leu | |
| ENST00000677039.1:n.3615C>T | ||
| ENST00000677399.1:n.1854C>T | ||
| ENST00000677496.1:c.1085C>T | ENSP00000504773.1:p.Pro362Leu | |
| ENST00000677517.1:c.1085C>T | ENSP00000503519.1:p.Pro362Leu | |
| ENST00000677633.1:c.*835C>T | ENSP00000503645.1:n.*835C>T | |
| ENST00000677800.1:c.*4516C>T | ENSP00000503794.1:n.*4516C>T | |
| ENST00000678057.1:c.*976C>T | ENSP00000503762.1:n.*976C>T | |
| ENST00000678119.1:n.1606C>T | ||
| ENST00000678166.1:n.1555C>T | ||
| ENST00000678312.1:n.1749C>T | ||
| ENST00000678316.1:c.*835C>T | ENSP00000504112.1:n.*835C>T | |
| ENST00000678371.1:n.1862C>T | ||
| ENST00000678404.1:c.1412C>T | ENSP00000503944.1:p.Pro471Leu | |
| ENST00000678419.1:c.1412C>T | ENSP00000504085.1:p.Pro471Leu | |
| ENST00000678433.1:n.1768C>T | ||
| ENST00000678467.1:c.1412C>T | ENSP00000504072.1:p.Pro471Leu | |
| ENST00000678569.1:c.*397C>T | ENSP00000504261.1:n.*397C>T | |
| ENST00000678961.1:n.1767C>T | ||
| ENST00000679002.1:n.1591C>T | ||
| ENST00000679012.1:c.968C>T | ENSP00000504446.1:p.Pro323Leu | |
| ENST00000679070.1:c.*831C>T | ENSP00000503759.1:n.*831C>T | |
| ENST00000679130.1:c.1412C>T | ENSP00000504845.1:p.Pro471Leu | |
| ENST00000679315.1:c.*1242C>T | ENSP00000503065.1:n.*1242C>T | |
| ENST00000243583.10:c.1289C>T | ENSP00000243583.5:p.Pro430Leu | |
| ENST00000324464.7:c.1412C>T | ENSP00000315118.3:p.Pro471Leu | |
| ENST00000593724.1:n.1527C>T | ||
| NM_001142555.2:c.1289C>T | NP_001136027.1:p.Pro430Leu | |
| NM_024876.3:c.1412C>T | NP_079152.3:p.Pro471Leu | |
| XM_005259270.3:c.1574C>T | XP_005259327.2:p.Pro525Leu | |
| XM_005259271.3:c.1412C>T | XP_005259328.1:p.Pro471Leu | |
| XM_005259272.3:c.1412C>T | XP_005259329.1:p.Pro471Leu | |
| XM_005259273.3:c.1412C>T | XP_005259330.1:p.Pro471Leu | |
| XM_006723392.2:c.1412C>T | XP_006723455.1:p.Pro471Leu | |
| XM_006723393.2:c.1412C>T | XP_006723456.1:p.Pro471Leu | |
| XM_011527334.1:c.1412C>T | XP_011525636.1:p.Pro471Leu | |
| XM_011527335.1:c.1271C>T | XP_011525637.1:p.Pro424Leu | |
| XM_011527336.1:c.1442C>T | XP_011525638.1:p.Pro481Leu | |
| XM_011527337.1:c.1412C>T | XP_011525639.1:p.Pro471Leu | |
| XM_011527338.1:c.1412C>T | XP_011525640.1:p.Pro471Leu | |
| NM_024876.4:c.1412C>T MANE Select | NP_079152.3:p.Pro471Leu | |
| NM_001142555.3:c.1289C>T | NP_001136027.1:p.Pro430Leu |