Canonical Allele Identifier: CA347952328
Gene: SLC9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1674803685

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532658G>T , CM000664.2:g.102532658G>T GRCh38
NC_000002.11:g.103149117G>T , CM000664.1:g.103149117G>T GRCh37
NC_000002.10:g.102515549G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2367G>T MANE Select ENSP00000295269.4:p.Arg789Ser
ENST00000295269.4:c.2367G>T ENSP00000295269.4:p.Arg789Ser
NM_001011552.3:c.2367G>T NP_001011552.2:p.Arg789Ser
XM_011511158.1:c.2280G>T XP_011509460.1:p.Arg760Ser
NM_001011552.4:c.2367G>T MANE Select NP_001011552.2:p.Arg789Ser