Canonical Allele Identifier: CA400784367
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs2060997267
gnomAD v4: 17-61590916-T-A
MyVariant Identifiers: chr17:g.59668277T>A (hg19) chr17:g.61590916T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590916T>A , CM000679.2:g.61590916T>A GRCh38
NC_000017.10:g.59668277T>A , CM000679.1:g.59668277T>A GRCh37
NC_000017.9:g.57023059T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.265A>T MANE Select ENSP00000427802.1:p.Thr89Ser
ENST00000521764.2:c.265A>T ENSP00000427802.1:p.Thr89Ser
NM_199290.3:c.265A>T NP_954984.1:p.Thr89Ser
NM_199290.4:c.265A>T MANE Select NP_954984.1:p.Thr89Ser
Search 100 bp 5'
Search 100 bp 3'