Canonical Allele Identifier: CA400784297
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668243T>A (hg19) chr17:g.61590882T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590882T>A , CM000679.2:g.61590882T>A GRCh38
NC_000017.10:g.59668243T>A , CM000679.1:g.59668243T>A GRCh37
NC_000017.9:g.57023025T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.299A>T MANE Select ENSP00000427802.1:p.Lys100Met
ENST00000521764.2:c.299A>T ENSP00000427802.1:p.Lys100Met
NM_199290.3:c.299A>T NP_954984.1:p.Lys100Met
NM_199290.4:c.299A>T MANE Select NP_954984.1:p.Lys100Met
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