Canonical Allele Identifier: CA501351125
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668260G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590899G>T , CM000679.2:g.61590899G>T GRCh38
NC_000017.10:g.59668260G>T , CM000679.1:g.59668260G>T GRCh37
NC_000017.9:g.57023042G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.282C>A MANE Select ENSP00000427802.1:p.Val94=
ENST00000521764.2:c.282C>A ENSP00000427802.1:p.Val94=
NM_199290.3:c.282C>A NP_954984.1:p.Val94=
NM_199290.4:c.282C>A MANE Select NP_954984.1:p.Val94=
Search 100 bp 5'
Search 100 bp 3'