Canonical Allele Identifier: CA107753950
Gene:

Linked Data

dbSNP Id: rs993838689

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601418C>G , CM000666.2:g.144601418C>G GRCh38
NC_000004.11:g.145522570C>G , CM000666.1:g.145522570C>G GRCh37
NC_000004.10:g.145742020C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-185440G>C ENSP00000497507.1:n.328-185440G>C