Canonical Allele Identifier: CA2772760663
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450211G>C , CM000668.2:g.117450211G>C GRCh38
NC_000006.11:g.117771374G>C , CM000668.1:g.117771374G>C GRCh37
NC_000006.10:g.117878067G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116643C>G ENSP00000487717.1:n.547+116643C>G