Canonical Allele Identifier: CA1697903983
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911550G= , CM000669.2:g.30911550G= GRCh38
NC_000007.13:g.30951165G= , CM000669.1:g.30951165G= GRCh37
NC_000007.12:g.30917690G= NCBI36
NG_007475.2:g.63157G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-443G=