Canonical Allele Identifier: CA2707245972
Gene:

Linked Data

dbSNP Id: rs1727413526

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601425G>C , CM000666.2:g.144601425G>C GRCh38
NC_000004.11:g.145522577G>C , CM000666.1:g.145522577G>C GRCh37
NC_000004.10:g.145742027G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185447C>G ENSP00000497507.1:n.328-185447C>G