Canonical Allele Identifier: CA2639246543
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498405A>C , CM000679.2:g.63498405A>C GRCh38
NC_000017.10:g.61575766A>C , CM000679.1:g.61575766A>C GRCh37
NC_000017.9:g.58929498A>C NCBI36
NG_011648.1:g.26333A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1420A>C ENSP00000464149.1:n.1969+1420A>C