Canonical Allele Identifier: CA812366537
Gene: C5orf67 HGNC NCBI

Linked Data

dbSNP Id: rs1461275032
gnomAD v3: 5-56564186-T-C
gnomAD v4: 5-56564186-T-C
MyVariant Identifiers: chr5:g.55860013T>C (hg19) chr5:g.56564186T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56564186T>C , CM000667.2:g.56564186T>C GRCh38
NC_000005.9:g.55860013T>C , CM000667.1:g.55860013T>C GRCh37
NC_000005.8:g.55895770T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438651.5:c.-15-7999A>G ENSP00000406718.1:n.-15-7999A>G
NM_001287053.1:c.-15-7999A>G NP_001273982.1:n.-15-7999A>G
XM_017008942.1:c.-16+6192A>G XP_016864431.1:n.-16+6192A>G
NR_161255.1:n.236-7999A>G
Search 100 bp 5'
Search 100 bp 3'