Canonical Allele Identifier: CA2572505116
Gene:

Linked Data

dbSNP Id: rs2126536941

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601498A>G , CM000666.2:g.144601498A>G GRCh38
NC_000004.11:g.145522650A>G , CM000666.1:g.145522650A>G GRCh37
NC_000004.10:g.145742100A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-185520T>C ENSP00000497507.1:n.328-185520T>C