Canonical Allele Identifier: CA292793859
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs951307026
gnomAD v4: 17-61590946-C-T
MyVariant Identifiers: chr17:g.59668307C>T (hg19) chr17:g.61590946C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590946C>T , CM000679.2:g.61590946C>T GRCh38
NC_000017.10:g.59668307C>T , CM000679.1:g.59668307C>T GRCh37
NC_000017.9:g.57023089C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.235G>A MANE Select ENSP00000427802.1:p.Ala79Thr
ENST00000521764.2:c.235G>A ENSP00000427802.1:p.Ala79Thr
NM_199290.3:c.235G>A NP_954984.1:p.Ala79Thr
NM_199290.4:c.235G>A MANE Select NP_954984.1:p.Ala79Thr
Search 100 bp 5'
Search 100 bp 3'