Canonical Allele Identifier: CA501351141
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668269A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590908A>G , CM000679.2:g.61590908A>G GRCh38
NC_000017.10:g.59668269A>G , CM000679.1:g.59668269A>G GRCh37
NC_000017.9:g.57023051A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.273T>C MANE Select ENSP00000427802.1:p.Val91=
ENST00000521764.2:c.273T>C ENSP00000427802.1:p.Val91=
NM_199290.3:c.273T>C NP_954984.1:p.Val91=
NM_199290.4:c.273T>C MANE Select NP_954984.1:p.Val91=
Search 100 bp 5'
Search 100 bp 3'