Canonical Allele Identifier: CA400784307
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668247A>T (hg19) chr17:g.61590886A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590886A>T , CM000679.2:g.61590886A>T GRCh38
NC_000017.10:g.59668247A>T , CM000679.1:g.59668247A>T GRCh37
NC_000017.9:g.57023029A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.295T>A MANE Select ENSP00000427802.1:p.Ser99Thr
ENST00000521764.2:c.295T>A ENSP00000427802.1:p.Ser99Thr
NM_199290.3:c.295T>A NP_954984.1:p.Ser99Thr
NM_199290.4:c.295T>A MANE Select NP_954984.1:p.Ser99Thr
Search 100 bp 5'
Search 100 bp 3'