Canonical Allele Identifier: CA1685476499
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs836478
gnomAD v4: 7-6392059-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392059C>G , CM000669.2:g.6392059C>G GRCh38
NC_000007.13:g.6431690C>G , CM000669.1:g.6431690C>G GRCh37
NC_000007.12:g.6398215C>G NCBI36
NG_029431.1:g.22565C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.431C>G
ENST00000704002.1:c.324+18C>G ENSP00000515615.1:n.324+18C>G
ENST00000704003.1:c.*178+18C>G ENSP00000515616.1:n.*178+18C>G
ENST00000348035.9:c.225+18C>G MANE Select ENSP00000258737.7:n.225+18C>G
ENST00000348035.8:c.225+18C>G ENSP00000258737.7:n.225+18C>G
ENST00000356142.4:c.225+18C>G ENSP00000348461.4:n.225+18C>G
ENST00000488373.5:n.456+18C>G
ENST00000497741.5:n.241+18C>G
NM_006908.4:c.225+18C>G NP_008839.2:n.225+18C>G
NM_018890.3:c.225+18C>G NP_061485.1:n.225+18C>G
NM_006908.5:c.225+18C>G MANE Select NP_008839.2:n.225+18C>G
NM_018890.4:c.225+18C>G NP_061485.1:n.225+18C>G