Canonical Allele Identifier: CA281436477
Gene:

Linked Data

dbSNP Id: rs1010038725

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655542A>G , CM000678.2:g.55655542A>G GRCh38
NC_000016.9:g.55689454A>G , CM000678.1:g.55689454A>G GRCh37
NC_000016.8:g.54246955A>G NCBI36
NG_016969.1:g.4913A>G

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+57T>C