Canonical Allele Identifier: CA427841215
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149012G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532553G>C , CM000664.2:g.102532553G>C GRCh38
NC_000002.11:g.103149012G>C , CM000664.1:g.103149012G>C GRCh37
NC_000002.10:g.102515444G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2262G>C MANE Select ENSP00000295269.4:p.Val754=
ENST00000295269.4:c.2262G>C ENSP00000295269.4:p.Val754=
NM_001011552.3:c.2262G>C NP_001011552.2:p.Val754=
XM_011511158.1:c.2175G>C XP_011509460.1:p.Val725=
NM_001011552.4:c.2262G>C MANE Select NP_001011552.2:p.Val754=
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