Canonical Allele Identifier: CA400784304
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668246G>A (hg19) chr17:g.61590885G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590885G>A , CM000679.2:g.61590885G>A GRCh38
NC_000017.10:g.59668246G>A , CM000679.1:g.59668246G>A GRCh37
NC_000017.9:g.57023028G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.296C>T MANE Select ENSP00000427802.1:p.Ser99Phe
ENST00000521764.2:c.296C>T ENSP00000427802.1:p.Ser99Phe
NM_199290.3:c.296C>T NP_954984.1:p.Ser99Phe
NM_199290.4:c.296C>T MANE Select NP_954984.1:p.Ser99Phe
Search 100 bp 5'
Search 100 bp 3'