Canonical Allele Identifier: CA2733905744
Gene:

Linked Data

dbSNP Id: rs2147591177

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506326A>G , CM000679.2:g.63506326A>G GRCh38
NC_000017.10:g.61583687A>G , CM000679.1:g.61583687A>G GRCh37
NC_000017.9:g.58937419A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577647.2:c.1970-730A>G ENSP00000464149.1:n.1970-730A>G