Canonical Allele Identifier: CA501351418

Gene: NACA2

Linked Data

• dbSNP Id: rs1417259288
• gnomAD v2: 17-59668104-T-C
• gnomAD v4: 17-61590743-T-C
• MyVariant Identifiers: chr17:g.59668104T>C (hg19) ; chr17:g.61590743T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61590743T>C , CM000679.2:g.61590743T>C	GRCh38
NC_000017.10:g.59668104T>C , CM000679.1:g.59668104T>C	GRCh37
NC_000017.9:g.57022886T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521764.3:c.438A>G MANE Select	ENSP00000427802.1:p.Gln146=
ENST00000521764.2:c.438A>G	ENSP00000427802.1:p.Gln146=
NM_199290.3:c.438A>G	NP_954984.1:p.Gln146=
NM_199290.4:c.438A>G MANE Select	NP_954984.1:p.Gln146=