Canonical Allele Identifier: CA8690153
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs764722535

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590529A>T , CM000679.2:g.61590529A>T GRCh38
NC_000017.10:g.59667890A>T , CM000679.1:g.59667890A>T GRCh37
NC_000017.9:g.57022672A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.*4T>A MANE Select ENSP00000427802.1:n.*4T>A
ENST00000521764.2:c.*4T>A ENSP00000427802.1:n.*4T>A
NM_199290.3:c.*4T>A NP_954984.1:n.*4T>A
NM_199290.4:c.*4T>A MANE Select NP_954984.1:n.*4T>A