Canonical Allele Identifier: CA14474086
Gene:

Linked Data

dbSNP Id: rs8073782

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27807685C>T , CM000679.2:g.27807685C>T GRCh38
NC_000017.10:g.26134711C>T , CM000679.1:g.26134711C>T GRCh37
NC_000017.9:g.23158838C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000582441.1:c.220-3344G>A ENSP00000462879.1:n.220-3344G>A