Canonical Allele Identifier: CA427841849
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149120C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532661C>T , CM000664.2:g.102532661C>T GRCh38
NC_000002.11:g.103149120C>T , CM000664.1:g.103149120C>T GRCh37
NC_000002.10:g.102515552C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2370C>T MANE Select ENSP00000295269.4:p.Ser790=
ENST00000295269.4:c.2370C>T ENSP00000295269.4:p.Ser790=
NM_001011552.3:c.2370C>T NP_001011552.2:p.Ser790=
XM_011511158.1:c.2283C>T XP_011509460.1:p.Ser761=
NM_001011552.4:c.2370C>T MANE Select NP_001011552.2:p.Ser790=
Search 100 bp 5'
Search 100 bp 3'