Canonical Allele Identifier: CA8690159
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs781705734

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590555G>A , CM000679.2:g.61590555G>A GRCh38
NC_000017.10:g.59667916G>A , CM000679.1:g.59667916G>A GRCh37
NC_000017.9:g.57022698G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.626C>T MANE Select ENSP00000427802.1:p.Ala209Val
ENST00000521764.2:c.626C>T ENSP00000427802.1:p.Ala209Val
NM_199290.3:c.626C>T NP_954984.1:p.Ala209Val
NM_199290.4:c.626C>T MANE Select NP_954984.1:p.Ala209Val