Canonical Allele Identifier: CA1697889771
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897620C= , CM000669.2:g.30897620C= GRCh38
NC_000007.13:g.30937235C= , CM000669.1:g.30937235C= GRCh37
NC_000007.12:g.30903760C= NCBI36
NG_007475.2:g.49227C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509504.2:c.622-14373C=