Canonical Allele Identifier: CA119466311
Gene: C5orf67 HGNC NCBI

Linked Data

dbSNP Id: rs936911512
gnomAD v3: 5-56572275-G-C
gnomAD v4: 5-56572275-G-C
MyVariant Identifiers: chr5:g.55868102G>C (hg19) chr5:g.56572275G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56572275G>C , CM000667.2:g.56572275G>C GRCh38
NC_000005.9:g.55868102G>C , CM000667.1:g.55868102G>C GRCh37
NC_000005.8:g.55903859G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438651.5:c.-15-16088C>G ENSP00000406718.1:n.-15-16088C>G
NM_001287053.1:c.-15-16088C>G NP_001273982.1:n.-15-16088C>G
XM_017008942.1:c.-628-395C>G XP_016864431.1:n.-628-395C>G
NR_161255.1:n.236-16088C>G
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