Canonical Allele Identifier: CA400784061
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs1603265776
gnomAD v4: 17-61590768-G-C
MyVariant Identifiers: chr17:g.59668129G>C (hg19) chr17:g.61590768G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590768G>C , CM000679.2:g.61590768G>C GRCh38
NC_000017.10:g.59668129G>C , CM000679.1:g.59668129G>C GRCh37
NC_000017.9:g.57022911G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.413C>G MANE Select ENSP00000427802.1:p.Ala138Gly
ENST00000521764.2:c.413C>G ENSP00000427802.1:p.Ala138Gly
NM_199290.3:c.413C>G NP_954984.1:p.Ala138Gly
NM_199290.4:c.413C>G MANE Select NP_954984.1:p.Ala138Gly
Search 100 bp 5'
Search 100 bp 3'