Canonical Allele Identifier: CA427841480
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149057T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532598T>G , CM000664.2:g.102532598T>G GRCh38
NC_000002.11:g.103149057T>G , CM000664.1:g.103149057T>G GRCh37
NC_000002.10:g.102515489T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2307T>G MANE Select ENSP00000295269.4:p.Ser769=
ENST00000295269.4:c.2307T>G ENSP00000295269.4:p.Ser769=
NM_001011552.3:c.2307T>G NP_001011552.2:p.Ser769=
XM_011511158.1:c.2220T>G XP_011509460.1:p.Ser740=
NM_001011552.4:c.2307T>G MANE Select NP_001011552.2:p.Ser769=
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