Canonical Allele Identifier: CA107971401
Gene:

Linked Data

dbSNP Id: rs769212077

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649535A>C , CM000666.2:g.148649535A>C GRCh38
NC_000004.11:g.149570687A>C , CM000666.1:g.149570687A>C GRCh37
NC_000004.10:g.149790137A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30667T>G
XR_001741441.1:n.1745+104951A>C
XR_939336.3:n.2921-30667T>G