Canonical Allele Identifier: CA1129362924
Gene:

Linked Data

dbSNP Id: rs1841645220

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945525A>G , CM000671.2:g.128945525A>G GRCh38
NC_000009.11:g.131707804A>G , CM000671.1:g.131707804A>G GRCh37
NC_000009.10:g.130747625A>G NCBI36
NG_017009.1:g.7209T>C , LRG_744:g.7209T>C
NG_033111.1:g.2833A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000482796.1:c.39-3664A>G ENSP00000417556.2:n.39-3664A>G