Canonical Allele Identifier: CA1697903982
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911544A= , CM000669.2:g.30911544A= GRCh38
NC_000007.13:g.30951159A= , CM000669.1:g.30951159A= GRCh37
NC_000007.12:g.30917684A= NCBI36
NG_007475.2:g.63151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-449A=