Canonical Allele Identifier: CA2269090978
Gene: NACA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590740A= , CM000679.2:g.61590740A= GRCh38
NC_000017.10:g.59668101A= , CM000679.1:g.59668101A= GRCh37
NC_000017.9:g.57022883A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.441T= MANE Select ENSP00000427802.1:p.Gly147=
ENST00000521764.2:c.441T= ENSP00000427802.1:p.Gly147=
NM_199290.3:c.441T= NP_954984.1:p.Gly147=
NM_199290.4:c.441T= MANE Select NP_954984.1:p.Gly147=