Canonical Allele Identifier: CA501351177
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668287A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590926A>C , CM000679.2:g.61590926A>C GRCh38
NC_000017.10:g.59668287A>C , CM000679.1:g.59668287A>C GRCh37
NC_000017.9:g.57023069A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.255T>G MANE Select ENSP00000427802.1:p.Leu85=
ENST00000521764.2:c.255T>G ENSP00000427802.1:p.Leu85=
NM_199290.3:c.255T>G NP_954984.1:p.Leu85=
NM_199290.4:c.255T>G MANE Select NP_954984.1:p.Leu85=
Search 100 bp 5'
Search 100 bp 3'