Canonical Allele Identifier: CA1069062008
Gene:

Linked Data

dbSNP Id: rs1578785965

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601554T>C , CM000666.2:g.144601554T>C GRCh38
NC_000004.11:g.145522706T>C , CM000666.1:g.145522706T>C GRCh37
NC_000004.10:g.145742156T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185576A>G ENSP00000497507.1:n.328-185576A>G