Canonical Allele Identifier: CA119464622
Gene: C5orf67 HGNC NCBI

Linked Data

dbSNP Id: rs778557452
MyVariant Identifiers: chr5:g.56564056C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56564056C>A , CM000667.2:g.56564056C>A GRCh38
NC_000005.9:g.55859883C>A , CM000667.1:g.55859883C>A GRCh37
NC_000005.8:g.55895640C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438651.5:c.-15-7869G>T ENSP00000406718.1:n.-15-7869G>T
NM_001287053.1:c.-15-7869G>T NP_001273982.1:n.-15-7869G>T
XM_017008942.1:c.-16+6322G>T XP_016864431.1:n.-16+6322G>T
NR_161255.1:n.236-7869G>T