Canonical Allele Identifier: CA15902810
Gene:

Linked Data

dbSNP Id: rs12449782

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498888G>A , CM000679.2:g.63498888G>A GRCh38
NC_000017.10:g.61576249G>A , CM000679.1:g.61576249G>A GRCh37
NC_000017.9:g.58929981G>A NCBI36
NG_011648.1:g.26816G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000577647.2:c.1969+1903G>A ENSP00000464149.1:n.1969+1903G>A