Canonical Allele Identifier: CA2772760661
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450141A>G , CM000668.2:g.117450141A>G GRCh38
NC_000006.11:g.117771304A>G , CM000668.1:g.117771304A>G GRCh37
NC_000006.10:g.117877997A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116713T>C ENSP00000487717.1:n.547+116713T>C