Canonical Allele Identifier: CA2269091055
Gene: NACA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590914T= , CM000679.2:g.61590914T= GRCh38
NC_000017.10:g.59668275T= , CM000679.1:g.59668275T= GRCh37
NC_000017.9:g.57023057T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.267A= MANE Select ENSP00000427802.1:p.Thr89=
ENST00000521764.2:c.267A= ENSP00000427802.1:p.Thr89=
NM_199290.3:c.267A= NP_954984.1:p.Thr89=
NM_199290.4:c.267A= MANE Select NP_954984.1:p.Thr89=