Canonical Allele Identifier: CA1697903744
Gene:

Linked Data

dbSNP Id: rs1011031322

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911426G>C , CM000669.2:g.30911426G>C GRCh38
NC_000007.13:g.30951041G>C , CM000669.1:g.30951041G>C GRCh37
NC_000007.12:g.30917566G>C NCBI36
NG_007475.2:g.63033G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-567G>C