Canonical Allele Identifier: CA1697889751
Gene:

Linked Data

dbSNP Id: rs1039541015

Genomic Alleles

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

Transcript Alleles

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