Canonical Allele Identifier: CA773806449

Gene: NACA2

Linked Data

• dbSNP Id: rs1377632031
• gnomAD v4: 17-61590517-A-T
• MyVariant Identifiers: chr17:g.59667878A>T (hg19) ; chr17:g.61590517A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61590517A>T , CM000679.2:g.61590517A>T	GRCh38
NC_000017.10:g.59667878A>T , CM000679.1:g.59667878A>T	GRCh37
NC_000017.9:g.57022660A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521764.3:c.*16T>A MANE Select	ENSP00000427802.1:n.*16T>A
ENST00000521764.2:c.*16T>A	ENSP00000427802.1:n.*16T>A
NM_199290.3:c.*16T>A	NP_954984.1:n.*16T>A
NM_199290.4:c.*16T>A MANE Select	NP_954984.1:n.*16T>A