Canonical Allele Identifier: CA427841645
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149087T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532628T>G , CM000664.2:g.102532628T>G GRCh38
NC_000002.11:g.103149087T>G , CM000664.1:g.103149087T>G GRCh37
NC_000002.10:g.102515519T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2337T>G MANE Select ENSP00000295269.4:p.Ala779=
ENST00000295269.4:c.2337T>G ENSP00000295269.4:p.Ala779=
NM_001011552.3:c.2337T>G NP_001011552.2:p.Ala779=
XM_011511158.1:c.2250T>G XP_011509460.1:p.Ala750=
NM_001011552.4:c.2337T>G MANE Select NP_001011552.2:p.Ala779=