Canonical Allele Identifier: CA501351172
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs2060995254
MyVariant Identifiers: chr17:g.59667939G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590578G>A , CM000679.2:g.61590578G>A GRCh38
NC_000017.10:g.59667939G>A , CM000679.1:g.59667939G>A GRCh37
NC_000017.9:g.57022721G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.603C>T MANE Select ENSP00000427802.1:p.Asn201=
ENST00000521764.2:c.603C>T ENSP00000427802.1:p.Asn201=
NM_199290.3:c.603C>T NP_954984.1:p.Asn201=
NM_199290.4:c.603C>T MANE Select NP_954984.1:p.Asn201=
Search 100 bp 5'
Search 100 bp 3'