Canonical Allele Identifier: CA501351493
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs1362093037

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590767T>G , CM000679.2:g.61590767T>G GRCh38
NC_000017.10:g.59668128T>G , CM000679.1:g.59668128T>G GRCh37
NC_000017.9:g.57022910T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.414A>C MANE Select ENSP00000427802.1:p.Ala138=
ENST00000521764.2:c.414A>C ENSP00000427802.1:p.Ala138=
NM_199290.3:c.414A>C NP_954984.1:p.Ala138=
NM_199290.4:c.414A>C MANE Select NP_954984.1:p.Ala138=