Canonical Allele Identifier: CA400783566
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59667902T>A (hg19) chr17:g.61590541T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590541T>A , CM000679.2:g.61590541T>A GRCh38
NC_000017.10:g.59667902T>A , CM000679.1:g.59667902T>A GRCh37
NC_000017.9:g.57022684T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.640A>T MANE Select ENSP00000427802.1:p.Thr214Ser
ENST00000521764.2:c.640A>T ENSP00000427802.1:p.Thr214Ser
NM_199290.3:c.640A>T NP_954984.1:p.Thr214Ser
NM_199290.4:c.640A>T MANE Select NP_954984.1:p.Thr214Ser
Search 100 bp 5'
Search 100 bp 3'