Canonical Allele Identifier: CA1697903759
Gene:

Linked Data

dbSNP Id: rs1791155775

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911429C>A , CM000669.2:g.30911429C>A GRCh38
NC_000007.13:g.30951044C>A , CM000669.1:g.30951044C>A GRCh37
NC_000007.12:g.30917569C>A NCBI36
NG_007475.2:g.63036C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-564C>A