Canonical Allele Identifier: CA52947141
Gene: SLC9A4 HGNC NCBI

Linked Data

dbSNP Id: rs915537834

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532471A>G , CM000664.2:g.102532471A>G GRCh38
NC_000002.11:g.103148930A>G , CM000664.1:g.103148930A>G GRCh37
NC_000002.10:g.102515362A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2180A>G MANE Select ENSP00000295269.4:p.Tyr727Cys
ENST00000295269.4:c.2180A>G ENSP00000295269.4:p.Tyr727Cys
NM_001011552.3:c.2180A>G NP_001011552.2:p.Tyr727Cys
XM_011511158.1:c.2093A>G XP_011509460.1:p.Tyr698Cys
NM_001011552.4:c.2180A>G MANE Select NP_001011552.2:p.Tyr727Cys