Canonical Allele Identifier: CA1697903750
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911428A= , CM000669.2:g.30911428A= GRCh38
NC_000007.13:g.30951043A= , CM000669.1:g.30951043A= GRCh37
NC_000007.12:g.30917568A= NCBI36
NG_007475.2:g.63035A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-565A=