Canonical Allele Identifier: CA1697889775
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897632C= , CM000669.2:g.30897632C= GRCh38
NC_000007.13:g.30937247C= , CM000669.1:g.30937247C= GRCh37
NC_000007.12:g.30903772C= NCBI36
NG_007475.2:g.49239C=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14361C=