Canonical Allele Identifier: CA1605800771
Community Standard Title: NC_000006.12:g.1573378G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1573378G= , CM000668.2:g.1573378G= GRCh38
NC_000006.11:g.1573613G= , CM000668.1:g.1573613G= GRCh37
NC_000006.10:g.1518612G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743924.1:n.86+6841C=