Canonical Allele Identifier: CA1697903932
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911511A= , CM000669.2:g.30911511A= GRCh38
NC_000007.13:g.30951126A= , CM000669.1:g.30951126A= GRCh37
NC_000007.12:g.30917651A= NCBI36
NG_007475.2:g.63118A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-482A=