Canonical Allele Identifier: CA1697889767
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897608A= , CM000669.2:g.30897608A= GRCh38
NC_000007.13:g.30937223A= , CM000669.1:g.30937223A= GRCh37
NC_000007.12:g.30903748A= NCBI36
NG_007475.2:g.49215A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14385A=