Canonical Allele Identifier: CA427841238
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149015T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532556T>C , CM000664.2:g.102532556T>C GRCh38
NC_000002.11:g.103149015T>C , CM000664.1:g.103149015T>C GRCh37
NC_000002.10:g.102515447T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2265T>C MANE Select ENSP00000295269.4:p.Asp755=
ENST00000295269.4:c.2265T>C ENSP00000295269.4:p.Asp755=
NM_001011552.3:c.2265T>C NP_001011552.2:p.Asp755=
XM_011511158.1:c.2178T>C XP_011509460.1:p.Asp726=
NM_001011552.4:c.2265T>C MANE Select NP_001011552.2:p.Asp755=
Search 100 bp 5'
Search 100 bp 3'