Canonical Allele Identifier: CA400784225
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs750498099

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590847A>T , CM000679.2:g.61590847A>T GRCh38
NC_000017.10:g.59668208A>T , CM000679.1:g.59668208A>T GRCh37
NC_000017.9:g.57022990A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.334T>A MANE Select ENSP00000427802.1:p.Tyr112Asn
ENST00000521764.2:c.334T>A ENSP00000427802.1:p.Tyr112Asn
NM_199290.3:c.334T>A NP_954984.1:p.Tyr112Asn
NM_199290.4:c.334T>A MANE Select NP_954984.1:p.Tyr112Asn