Canonical Allele Identifier: CA2269090889
Gene: NACA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590573C= , CM000679.2:g.61590573C= GRCh38
NC_000017.10:g.59667934C= , CM000679.1:g.59667934C= GRCh37
NC_000017.9:g.57022716C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.608G= MANE Select ENSP00000427802.1:p.Ser203=
ENST00000521764.2:c.608G= ENSP00000427802.1:p.Ser203=
NM_199290.3:c.608G= NP_954984.1:p.Ser203=
NM_199290.4:c.608G= MANE Select NP_954984.1:p.Ser203=