Canonical Allele Identifier: CA1284431694
Gene:

Linked Data

dbSNP Id: rs1678947917

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368976T>C , CM000664.2:g.122368976T>C GRCh38
NC_000002.11:g.123126552T>C , CM000664.1:g.123126552T>C GRCh37
NC_000002.10:g.122843022T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-23987T>C
XR_001739684.1:n.556-23987T>C