Canonical Allele Identifier: CA2766889313
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70049520A>C , CM000667.2:g.70049520A>C GRCh38
NC_000005.9:g.69345347A>C , CM000667.1:g.69345347A>C GRCh37
NC_000005.8:g.69381103A>C NCBI36
NG_008728.1:g.4998A>C

Transcript Alleles

HGVS Amino-acid Change
XR_948432.1:n.1054+61516A>C