Canonical Allele Identifier: CA347951985
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149003T>G (hg19) chr2:g.102532544T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532544T>G , CM000664.2:g.102532544T>G GRCh38
NC_000002.11:g.103149003T>G , CM000664.1:g.103149003T>G GRCh37
NC_000002.10:g.102515435T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2253T>G MANE Select ENSP00000295269.4:p.Phe751Leu
ENST00000295269.4:c.2253T>G ENSP00000295269.4:p.Phe751Leu
NM_001011552.3:c.2253T>G NP_001011552.2:p.Phe751Leu
XM_011511158.1:c.2166T>G XP_011509460.1:p.Phe722Leu
NM_001011552.4:c.2253T>G MANE Select NP_001011552.2:p.Phe751Leu
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