Canonical Allele Identifier: CA837538778
Gene:

Linked Data

dbSNP Id: rs1420368260

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897578C>T , CM000669.2:g.30897578C>T GRCh38
NC_000007.13:g.30937193C>T , CM000669.1:g.30937193C>T GRCh37
NC_000007.12:g.30903718C>T NCBI36
NG_007475.2:g.49185C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14415C>T