Canonical Allele Identifier: CA1649549850
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98128347G= , CM000668.2:g.98128347G= GRCh38
NC_000006.11:g.98576223G= , CM000668.1:g.98576223G= GRCh37
NC_000006.10:g.98682944G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942809.1:n.456+29077G=