Canonical Allele Identifier: CA1915219147
Gene:

Linked Data

dbSNP Id: rs938036

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.63898984T>G , CM000672.2:g.63898984T>G GRCh38
NC_000010.10:g.65658744T>G , CM000672.1:g.65658744T>G GRCh37
NC_000010.9:g.65328750T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946010.1:n.275+11308T>G
XR_946011.1:n.275+11308T>G
XR_946012.1:n.275+11308T>G
XR_946013.1:n.275+11308T>G