Linked Data
ClinVar Variation Id:
1980700
ClinVar RCV Id:
RCV002780313
dbSNP Id:
rs763667541
ExAC:
19:15298121 G / A
gnomAD v2:
19-15298121-G-A
gnomAD v4:
19-15187310-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15187310G>A , CM000681.2:g.15187310G>A | GRCh38 |
| NC_000019.9:g.15298121G>A , CM000681.1:g.15298121G>A | GRCh37 |
| NC_000019.8:g.15159121G>A | NCBI36 |
| NG_009819.1:g.18672C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.1635C>T MANE Select | ENSP00000263388.1:p.Asn545= | |
| ENST00000263388.6:c.1635C>T | ENSP00000263388.1:p.Asn545= | |
| ENST00000601011.1:c.1632C>T | ENSP00000473138.1:p.Asn544= | |
| NM_000435.2:c.1635C>T | NP_000426.2:p.Asn545= | |
| XM_005259924.3:c.1635C>T | XP_005259981.1:p.Asn545= | |
| XM_005259924.4:c.1635C>T | XP_005259981.1:p.Asn545= | |
| NM_000435.3:c.1635C>T MANE Select | NP_000426.2:p.Asn545= |