Canonical Allele Identifier: CA13398760
Gene: FXYD6-FXYD2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10790212

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117831975C>T , CM000673.2:g.117831975C>T GRCh38
NC_000011.9:g.117702690C>T , CM000673.1:g.117702690C>T GRCh37
NC_000011.8:g.117207900C>T NCBI36
NG_011543.1:g.1118G>A

Transcript Alleles

HGVS Amino-acid change
NM_001204268.1:c.259+7806G>A VV NP_001191197.1:p.=
NM_001243598.2:c.272+7806G>A VV NP_001230527.1:p.=
ENST00000532984.1:c.272+7806G>A ENSP00000463024.1:p.=
ENST00000614497.5:c.259+7806G>A ENSP00000482442.1:p.=