Canonical Allele Identifier: CA107754195
Gene:

Linked Data

dbSNP Id: rs896208052

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601681A>G , CM000666.2:g.144601681A>G GRCh38
NC_000004.11:g.145522833A>G , CM000666.1:g.145522833A>G GRCh37
NC_000004.10:g.145742283A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185703T>C ENSP00000497507.1:n.328-185703T>C