Canonical Allele Identifier: CA622292852
Gene:

Linked Data

dbSNP Id: rs1461668555

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655541T>C , CM000678.2:g.55655541T>C GRCh38
NC_000016.9:g.55689453T>C , CM000678.1:g.55689453T>C GRCh37
NC_000016.8:g.54246954T>C NCBI36
NG_016969.1:g.4912T>C

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+58A>G