Linked Data
ClinVar Variation Id:
449260
dbSNP Id:
rs574863380
ExAC:
6:75855168 G / A
gnomAD v2:
6-75855168-G-A
gnomAD v3:
6-75145452-G-A
gnomAD v4:
6-75145452-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.75145452G>A , CM000668.2:g.75145452G>A | GRCh38 |
| NC_000006.11:g.75855168G>A , CM000668.1:g.75855168G>A | GRCh37 |
| NC_000006.10:g.75911888G>A | NCBI36 |
| NG_042181.1:g.65456C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322507.13:c.4564C>T MANE Select | ENSP00000325146.8:p.Arg1522Cys | |
| ENST00000322507.12:c.4564C>T | ENSP00000325146.8:p.Arg1522Cys | |
| ENST00000345356.10:c.1072C>T | ENSP00000305147.9:p.Arg358Cys | |
| ENST00000416123.6:c.4564C>T | ENSP00000412864.2:p.Arg1522Cys | |
| ENST00000419671.1:c.788C>T | ||
| ENST00000474564.1:n.188C>T | ||
| ENST00000483888.6:c.4564C>T | ENSP00000421216.1:p.Arg1522Cys | |
| ENST00000615798.4:c.997C>T | ENSP00000483232.1:p.Arg333Cys | |
| NM_004370.5:c.4564C>T | NP_004361.3:p.Arg1522Cys | |
| NM_080645.2:c.1072C>T | NP_542376.2:p.Arg358Cys | |
| XM_011535434.1:c.4564C>T | XP_011533736.1:p.Arg1522Cys | |
| XM_011535435.1:c.4291C>T | XP_011533737.1:p.Arg1431Cys | |
| XM_011535436.1:c.1072C>T | XP_011533738.1:p.Arg358Cys | |
| XM_011535436.2:c.1072C>T | XP_011533738.1:p.Arg358Cys | |
| XM_017010252.2:c.4528C>T | XP_016865741.1:p.Arg1510Cys | |
| NM_004370.6:c.4564C>T MANE Select | NP_004361.3:p.Arg1522Cys | |
| NM_080645.3:c.1072C>T | NP_542376.2:p.Arg358Cys |