Canonical Allele Identifier: CA404906846
Gene: NCAN HGNC NCBI

Linked Data

dbSNP Id: rs1190504050
gnomAD v2: 19-19329825-T-C
gnomAD v4: 19-19219016-T-C
MyVariant Identifiers: chr19:g.19329825T>C (hg19) chr19:g.19219016T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19219016T>C , CM000681.2:g.19219016T>C GRCh38
NC_000019.9:g.19329825T>C , CM000681.1:g.19329825T>C GRCh37
NC_000019.8:g.19190825T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252575.11:c.175T>C MANE Select ENSP00000252575.4:p.Cys59Arg
ENST00000252575.10:c.175T>C ENSP00000252575.4:p.Cys59Arg
NM_004386.2:c.175T>C NP_004377.2:p.Cys59Arg
XM_005259747.1:c.175T>C XP_005259804.1:p.Cys59Arg
NM_004386.3:c.175T>C MANE Select NP_004377.2:p.Cys59Arg
Search 100 bp 5'
Search 100 bp 3'