Canonical Allele Identifier: CA1275308283
Gene: SLC9A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532654A= , CM000664.2:g.102532654A= GRCh38
NC_000002.11:g.103149113A= , CM000664.1:g.103149113A= GRCh37
NC_000002.10:g.102515545A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2363A= MANE Select ENSP00000295269.4:p.His788=
ENST00000295269.4:c.2363A= ENSP00000295269.4:p.His788=
NM_001011552.3:c.2363A= NP_001011552.2:p.His788=
XM_011511158.1:c.2276A= XP_011509460.1:p.His759=
NM_001011552.4:c.2363A= MANE Select NP_001011552.2:p.His788=