Linked Data
ClinVar Variation Id:
210755
dbSNP Id:
rs35331711
ExAC:
3:148917570 G / A
gnomAD v2:
3-148917570-G-A
gnomAD v3:
3-149199783-G-A
gnomAD v4:
3-149199783-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.149199783G>A , CM000665.2:g.149199783G>A | GRCh38 |
| NC_000003.11:g.148917570G>A , CM000665.1:g.148917570G>A | GRCh37 |
| NC_000003.10:g.150400260G>A | NCBI36 |
| NG_011800.1:g.27263C>T | |
| NG_011800.2:g.27263C>T | |
| NG_011800.3:g.27263C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264613.11:c.1430C>T MANE Select | ENSP00000264613.6:p.Pro477Leu | |
| ENST00000264613.10:c.1430C>T | ENSP00000264613.6:p.Pro477Leu | |
| ENST00000471356.1:n.249C>T | ||
| ENST00000481169.5:c.1430C>T | ENSP00000418773.1:p.Pro477Leu | |
| ENST00000489736.5:n.655C>T | ||
| ENST00000490639.5:n.1462C>T | ||
| ENST00000494544.1:c.779C>T | ENSP00000420545.1:p.Pro260Leu | |
| ENST00000497797.5:n.39C>T | ||
| NM_000096.3:c.1430C>T | NP_000087.1:p.Pro477Leu | |
| NR_046371.1:n.1683C>T | ||
| XM_006713499.2:c.1430C>T | XP_006713562.1:p.Pro477Leu | |
| XM_006713500.2:c.1430C>T | XP_006713563.1:p.Pro477Leu | |
| XM_006713501.2:c.1430C>T | XP_006713564.1:p.Pro477Leu | |
| XM_006713502.2:c.1430C>T | XP_006713565.1:p.Pro477Leu | |
| XM_011512435.1:c.1430C>T | XP_011510737.1:p.Pro477Leu | |
| XR_427361.2:n.1688C>T | ||
| XM_006713499.3:c.1430C>T | XP_006713562.1:p.Pro477Leu | |
| XM_006713500.4:c.1430C>T | XP_006713563.1:p.Pro477Leu | |
| XM_006713501.3:c.1430C>T | XP_006713564.1:p.Pro477Leu | |
| XM_011512435.2:c.1430C>T | XP_011510737.1:p.Pro477Leu | |
| XM_017005734.2:c.1430C>T | XP_016861223.1:p.Pro477Leu | |
| XM_017005735.2:c.1430C>T | XP_016861224.1:p.Pro477Leu | |
| XR_427361.3:n.1646C>T | ||
| NM_000096.4:c.1430C>T MANE Select | NP_000087.2:p.Pro477Leu | |
| NR_046371.2:n.1467C>T |