Canonical Allele Identifier: CA292793854
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs966747690

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590921T>C , CM000679.2:g.61590921T>C GRCh38
NC_000017.10:g.59668282T>C , CM000679.1:g.59668282T>C GRCh37
NC_000017.9:g.57023064T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.260A>G MANE Select ENSP00000427802.1:p.Gln87Arg
ENST00000521764.2:c.260A>G ENSP00000427802.1:p.Gln87Arg
NM_199290.3:c.260A>G NP_954984.1:p.Gln87Arg
NM_199290.4:c.260A>G MANE Select NP_954984.1:p.Gln87Arg