Canonical Allele Identifier: CA12230602
Gene:

Linked Data

dbSNP Id: rs1265159

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31172270G>A , CM000668.2:g.31172270G>A GRCh38
NC_000006.11:g.31140047G>A , CM000668.1:g.31140047G>A GRCh37
NC_000006.10:g.31248026G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000441888.7:c.-183-6223C>T ENSP00000389359.2:p.=