Canonical Allele Identifier: CA400784466
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs1603265818
gnomAD v4: 17-61590965-A-C
MyVariant Identifiers: chr17:g.59668326A>C (hg19) chr17:g.61590965A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590965A>C , CM000679.2:g.61590965A>C GRCh38
NC_000017.10:g.59668326A>C , CM000679.1:g.59668326A>C GRCh37
NC_000017.9:g.57023108A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.216T>G MANE Select ENSP00000427802.1:p.Ser72Arg
ENST00000521764.2:c.216T>G ENSP00000427802.1:p.Ser72Arg
NM_199290.3:c.216T>G NP_954984.1:p.Ser72Arg
NM_199290.4:c.216T>G MANE Select NP_954984.1:p.Ser72Arg
Search 100 bp 5'
Search 100 bp 3'