Canonical Allele Identifier: CA1697903745
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911426G= , CM000669.2:g.30911426G= GRCh38
NC_000007.13:g.30951041G= , CM000669.1:g.30951041G= GRCh37
NC_000007.12:g.30917566G= NCBI36
NG_007475.2:g.63033G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-567G=