Canonical Allele Identifier: CA16194482
Gene: C4orf54 HGNC NCBI

Linked Data

dbSNP Id: rs11735070
gnomAD v3: 4-99792608-G-C
gnomAD v4: 4-99792608-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99792608G>C , CM000666.2:g.99792608G>C GRCh38
NC_000004.11:g.100713765G>C , CM000666.1:g.100713765G>C GRCh37
NC_000004.10:g.100932788G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_006714431.1:c.-32+29035C>G XP_006714494.1:n.-32+29035C>G