Canonical Allele Identifier: CA1275308290
Gene: SLC9A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532663A= , CM000664.2:g.102532663A= GRCh38
NC_000002.11:g.103149122A= , CM000664.1:g.103149122A= GRCh37
NC_000002.10:g.102515554A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2372A= MANE Select ENSP00000295269.4:p.His791=
ENST00000295269.4:c.2372A= ENSP00000295269.4:p.His791=
NM_001011552.3:c.2372A= NP_001011552.2:p.His791=
XM_011511158.1:c.2285A= XP_011509460.1:p.His762=
NM_001011552.4:c.2372A= MANE Select NP_001011552.2:p.His791=