Canonical Allele Identifier: CA427841689
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149096A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532637A>G , CM000664.2:g.102532637A>G GRCh38
NC_000002.11:g.103149096A>G , CM000664.1:g.103149096A>G GRCh37
NC_000002.10:g.102515528A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2346A>G MANE Select ENSP00000295269.4:p.Gly782=
ENST00000295269.4:c.2346A>G ENSP00000295269.4:p.Gly782=
NM_001011552.3:c.2346A>G NP_001011552.2:p.Gly782=
XM_011511158.1:c.2259A>G XP_011509460.1:p.Gly753=
NM_001011552.4:c.2346A>G MANE Select NP_001011552.2:p.Gly782=
Search 100 bp 5'
Search 100 bp 3'