Canonical Allele Identifier: CA1697903980
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911543G= , CM000669.2:g.30911543G= GRCh38
NC_000007.13:g.30951158G= , CM000669.1:g.30951158G= GRCh37
NC_000007.12:g.30917683G= NCBI36
NG_007475.2:g.63150G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-450G=