Canonical Allele Identifier: CA400784257

Gene: NACA2

Linked Data

• dbSNP Id: rs1315825833
• MyVariant Identifiers: chr17:g.59668225A>G (hg19) ; chr17:g.61590864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61590864A>G , CM000679.2:g.61590864A>G	GRCh38
NC_000017.10:g.59668225A>G , CM000679.1:g.59668225A>G	GRCh37
NC_000017.9:g.57023007A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521764.3:c.317T>C MANE Select	ENSP00000427802.1:p.Ile106Thr
ENST00000521764.2:c.317T>C	ENSP00000427802.1:p.Ile106Thr
NM_199290.3:c.317T>C	NP_954984.1:p.Ile106Thr
NM_199290.4:c.317T>C MANE Select	NP_954984.1:p.Ile106Thr