Canonical Allele Identifier: CA8690159

Gene: NACA2

Linked Data

• dbSNP Id: rs781705734
• ExAC: 17:59667916 G / A
• gnomAD v2: 17-59667916-G-A
• gnomAD v3: 17-61590555-G-A
• gnomAD v4: 17-61590555-G-A
• MyVariant Identifiers: chr17:g.59667916G>A (hg19) ; chr17:g.61590555G>A (hg38)

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