Canonical Allele Identifier: CA400784391
Gene: NACA2 HGNC NCBI

Linked Data

gnomAD v4: 17-61590928-G-C
MyVariant Identifiers: chr17:g.59668289G>C (hg19) chr17:g.61590928G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590928G>C , CM000679.2:g.61590928G>C GRCh38
NC_000017.10:g.59668289G>C , CM000679.1:g.59668289G>C GRCh37
NC_000017.9:g.57023071G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.253C>G MANE Select ENSP00000427802.1:p.Leu85Val
ENST00000521764.2:c.253C>G ENSP00000427802.1:p.Leu85Val
NM_199290.3:c.253C>G NP_954984.1:p.Leu85Val
NM_199290.4:c.253C>G MANE Select NP_954984.1:p.Leu85Val
Search 100 bp 5'
Search 100 bp 3'