Canonical Allele Identifier: CA2697151125
Gene:

Linked Data

dbSNP Id: rs2101527970

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147089055G>A , CM000663.2:g.147089055G>A GRCh38
NC_000001.10:g.146560602G>A , CM000663.1:g.146560602G>A GRCh37
NC_000001.9:g.145027226G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000444082.1:n.1845+20807C>T