Canonical Allele Identifier: CA119464654
Gene: C5orf67 HGNC NCBI

Linked Data

dbSNP Id: rs770418704
MyVariant Identifiers: chr5:g.55860014A>G (hg19) chr5:g.56564187A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56564187A>G , CM000667.2:g.56564187A>G GRCh38
NC_000005.9:g.55860014A>G , CM000667.1:g.55860014A>G GRCh37
NC_000005.8:g.55895771A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438651.5:c.-15-8000T>C ENSP00000406718.1:n.-15-8000T>C
NM_001287053.1:c.-15-8000T>C NP_001273982.1:n.-15-8000T>C
XM_017008942.1:c.-16+6191T>C XP_016864431.1:n.-16+6191T>C
NR_161255.1:n.236-8000T>C
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