Canonical Allele Identifier: CA2714349771
Gene:

Linked Data

dbSNP Id: rs2128587758

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911506C>T , CM000669.2:g.30911506C>T GRCh38
NC_000007.13:g.30951121C>T , CM000669.1:g.30951121C>T GRCh37
NC_000007.12:g.30917646C>T NCBI36
NG_007475.2:g.63113C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-487C>T