Canonical Allele Identifier: CA400784054
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668126G>C (hg19) chr17:g.61590765G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590765G>C , CM000679.2:g.61590765G>C GRCh38
NC_000017.10:g.59668126G>C , CM000679.1:g.59668126G>C GRCh37
NC_000017.9:g.57022908G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.416C>G MANE Select ENSP00000427802.1:p.Ala139Gly
ENST00000521764.2:c.416C>G ENSP00000427802.1:p.Ala139Gly
NM_199290.3:c.416C>G NP_954984.1:p.Ala139Gly
NM_199290.4:c.416C>G MANE Select NP_954984.1:p.Ala139Gly
Search 100 bp 5'
Search 100 bp 3'