Canonical Allele Identifier: CA2269091050
Gene: NACA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590900A= , CM000679.2:g.61590900A= GRCh38
NC_000017.10:g.59668261A= , CM000679.1:g.59668261A= GRCh37
NC_000017.9:g.57023043A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.281T= MANE Select ENSP00000427802.1:p.Val94=
ENST00000521764.2:c.281T= ENSP00000427802.1:p.Val94=
NM_199290.3:c.281T= NP_954984.1:p.Val94=
NM_199290.4:c.281T= MANE Select NP_954984.1:p.Val94=