Canonical Allele Identifier: CA12187075
Gene: HCG22 HGNC NCBI

Linked Data

dbSNP Id: rs9262632
gnomAD v2: 6-31024808-A-G
gnomAD v3: 6-31057031-A-G
gnomAD v4: 6-31057031-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31057031A>G , CM000668.2:g.31057031A>G GRCh38
NC_000006.11:g.31024808A>G , CM000668.1:g.31024808A>G GRCh37
NC_000006.10:g.31132787A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000646461.3:c.876+121A>G ENSP00000507162.2:n.876+121A>G
ENST00000426185.1:n.1511+121A>G
ENST00000565192.1:n.1192+121A>G
ENST00000566475.1:n.300-2377A>G
NR_003948.2:n.1700+121A>G
NR_145427.1:n.1192+121A>G
NR_003948.3:n.1701+121A>G
NR_145427.2:n.1193+121A>G