Linked Data
dbSNP Id:
rs2072901887
gnomAD v3:
15-74180140-G-A
gnomAD v4:
15-74180140-G-A
MyVariant Identifiers:
chr15:g.74472481G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74180140G>A , CM000677.2:g.74180140G>A | GRCh38 |
| NC_000015.9:g.74472481G>A , CM000677.1:g.74472481G>A | GRCh37 |
| NC_000015.8:g.72259534G>A | NCBI36 |
| NG_009207.1:g.33891C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395105.9:c.1944C>T MANE Select | ENSP00000378537.4:p.Asn648= | |
| ENST00000323940.9:c.1944C>T | ENSP00000326085.5:p.Asn648= | |
| ENST00000395105.8:c.1944C>T | ENSP00000378537.4:p.Asn648= | |
| ENST00000416286.7:c.1920C>T | ENSP00000400403.3:p.Asn640= | |
| ENST00000423167.6:c.1917C>T | ENSP00000413012.2:p.Asn639= | |
| ENST00000449139.6:c.1944C>T | ENSP00000410221.2:p.Asn648= | |
| ENST00000535552.5:c.2055C>T | ENSP00000440238.1:p.Asn685= | |
| ENST00000545137.5:n.1653C>T | ||
| ENST00000563965.5:c.2061C>T | ENSP00000456609.1:p.Asn687= | |
| ENST00000574278.5:c.1989C>T | ENSP00000458827.1:p.Asn663= | |
| ENST00000574439.5:n.2216C>T | ||
| ENST00000616000.4:c.1944C>T | ENSP00000479112.1:p.Asn648= | |
| NM_001142617.1:c.1944C>T | NP_001136089.1:p.Asn648= | |
| NM_001142618.1:c.1944C>T | NP_001136090.1:p.Asn648= | |
| NM_001142619.1:c.1917C>T | NP_001136091.1:p.Asn639= | |
| NM_001199040.1:c.2055C>T | NP_001185969.1:p.Asn685= | |
| NM_001199041.1:c.1989C>T | NP_001185970.1:p.Asn663= | |
| NM_001199042.1:c.2061C>T | NP_001185971.1:p.Asn687= | |
| NM_022369.3:c.1944C>T | NP_071764.3:p.Asn648= | |
| XM_011521883.1:c.1944C>T | XP_011520185.1:p.Asn648= | |
| XM_011521884.1:c.1755C>T | XP_011520186.1:p.Asn585= | |
| XM_017022478.1:c.1992C>T | XP_016877967.1:p.Asn664= | |
| XM_017022479.1:c.1944C>T | XP_016877968.1:p.Asn648= | |
| XM_017022480.1:c.1755C>T | XP_016877969.1:p.Asn585= | |
| NM_022369.4:c.1944C>T MANE Select | NP_071764.3:p.Asn648= | |
| NM_001142617.2:c.1944C>T | NP_001136089.1:p.Asn648= | |
| NM_001142619.2:c.1917C>T | NP_001136091.1:p.Asn639= | |
| NM_001199042.2:c.2061C>T | NP_001185971.1:p.Asn687= | |
| NM_001142618.2:c.1944C>T | NP_001136090.1:p.Asn648= | |
| NM_001199040.2:c.2055C>T | NP_001185969.1:p.Asn685= | |
| NM_001199041.2:c.1989C>T | NP_001185970.1:p.Asn663= |