Canonical Allele Identifier: CA156094451
Gene:

Linked Data

dbSNP Id: rs1039541015

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897581T>G , CM000669.2:g.30897581T>G GRCh38
NC_000007.13:g.30937196T>G , CM000669.1:g.30937196T>G GRCh37
NC_000007.12:g.30903721T>G NCBI36
NG_007475.2:g.49188T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14412T>G