Canonical Allele Identifier: CA347951994
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149007G>T (hg19) chr2:g.102532548G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532548G>T , CM000664.2:g.102532548G>T GRCh38
NC_000002.11:g.103149007G>T , CM000664.1:g.103149007G>T GRCh37
NC_000002.10:g.102515439G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2257G>T MANE Select ENSP00000295269.4:p.Ala753Ser
ENST00000295269.4:c.2257G>T ENSP00000295269.4:p.Ala753Ser
NM_001011552.3:c.2257G>T NP_001011552.2:p.Ala753Ser
XM_011511158.1:c.2170G>T XP_011509460.1:p.Ala724Ser
NM_001011552.4:c.2257G>T MANE Select NP_001011552.2:p.Ala753Ser
Search 100 bp 5'
Search 100 bp 3'