Linked Data
ClinVar Variation Id:
8035
ClinVar RCV Id:
RCV000008500
dbSNP Id:
rs121434494
ExAC:
19:18186622 G / A
gnomAD v2:
19-18186622-G-A
gnomAD v4:
19-18075812-G-A
PubMed:
PMID:11424023
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18075812G>A , CM000681.2:g.18075812G>A | GRCh38 |
| NC_000019.9:g.18186622G>A , CM000681.1:g.18186622G>A | GRCh37 |
| NC_000019.8:g.18047622G>A | NCBI36 |
| NG_007366.2:g.28138C>T , LRG_72:g.28138C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000593993.7:c.637C>T MANE Select | ENSP00000472165.2:p.Arg213Trp | |
| ENST00000322153.11:c.637C>T | ENSP00000314425.5:p.Arg213Trp | |
| ENST00000593993.6:c.637C>T | ENSP00000472165.2:p.Arg213Trp | |
| ENST00000600835.6:c.637C>T | ENSP00000470788.1:p.Arg213Trp | |
| NM_001290023.1:c.637C>T | NP_001276952.1:p.Arg213Trp | |
| NM_001290024.1:c.757C>T | NP_001276953.1:p.Arg253Trp | |
| NM_005535.2:c.637C>T | NP_005526.1:p.Arg213Trp | |
| NM_153701.2:c.637C>T | NP_714912.1:p.Arg213Trp | |
| XM_006722741.2:c.757C>T | XP_006722804.2:p.Arg253Trp | |
| XM_011527966.1:c.769C>T | XP_011526268.1:p.Arg257Trp | |
| XM_011527967.1:c.757C>T | XP_011526269.1:p.Arg253Trp | |
| XM_011527968.1:c.769C>T | XP_011526270.1:p.Arg257Trp | |
| XM_011527969.1:c.757C>T | XP_011526271.1:p.Arg253Trp | |
| XM_011527970.1:c.769C>T | XP_011526272.1:p.Arg257Trp | |
| XM_011527971.1:c.769C>T | XP_011526273.1:p.Arg257Trp | |
| XM_011527972.1:c.769C>T | XP_011526274.1:p.Arg257Trp | |
| XM_011527973.1:c.649C>T | XP_011526275.1:p.Arg217Trp | |
| XM_011527974.1:c.637C>T | XP_011526276.1:p.Arg213Trp | |
| XM_011527975.1:c.757C>T | XP_011526277.1:p.Arg253Trp | |
| XM_011527976.1:c.769C>T | XP_011526278.1:p.Arg257Trp | |
| XM_011527977.1:c.757C>T | XP_011526279.1:p.Arg253Trp | |
| XM_006722741.3:c.757C>T | XP_006722804.2:p.Arg253Trp | |
| XM_011527966.2:c.769C>T | XP_011526268.1:p.Arg257Trp | |
| XM_011527967.2:c.757C>T | XP_011526269.1:p.Arg253Trp | |
| XM_011527968.3:c.769C>T | XP_011526270.1:p.Arg257Trp | |
| XM_011527969.2:c.757C>T | XP_011526271.1:p.Arg253Trp | |
| XM_011527970.2:c.769C>T | XP_011526272.1:p.Arg257Trp | |
| XM_011527971.3:c.769C>T | XP_011526273.1:p.Arg257Trp | |
| XM_011527972.3:c.769C>T | XP_011526274.1:p.Arg257Trp | |
| XM_011527973.2:c.649C>T | XP_011526275.1:p.Arg217Trp | |
| XM_011527974.2:c.637C>T | XP_011526276.1:p.Arg213Trp | |
| XM_011527975.2:c.757C>T | XP_011526277.1:p.Arg253Trp | |
| XM_011527976.2:c.769C>T | XP_011526278.1:p.Arg257Trp | |
| XM_011527977.2:c.757C>T | XP_011526279.1:p.Arg253Trp | |
| XM_017026762.1:c.34C>T | XP_016882251.1:p.Arg12Trp | |
| NM_001290023.2:c.637C>T | NP_001276952.1:p.Arg213Trp | |
| NM_005535.3:c.637C>T MANE Select | NP_005526.1:p.Arg213Trp | |
| NM_153701.3:c.637C>T | NP_714912.1:p.Arg213Trp |