Canonical Allele Identifier: CA281436480
Gene:

Linked Data

dbSNP Id: rs1018788214

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655560T>C , CM000678.2:g.55655560T>C GRCh38
NC_000016.9:g.55689472T>C , CM000678.1:g.55689472T>C GRCh37
NC_000016.8:g.54246973T>C NCBI36
NG_016969.1:g.4931T>C

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+39A>G