Canonical Allele Identifier: CA1697903720
Gene:

Linked Data

dbSNP Id: rs1791155184

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911415G>A , CM000669.2:g.30911415G>A GRCh38
NC_000007.13:g.30951030G>A , CM000669.1:g.30951030G>A GRCh37
NC_000007.12:g.30917555G>A NCBI36
NG_007475.2:g.63022G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-578G>A