Canonical Allele Identifier: CA137969593
Gene: ADGRF4 HGNC NCBI

Linked Data

dbSNP Id: rs937888864
gnomAD v2: 6-47678213-A-G
gnomAD v3: 6-47710477-A-G
gnomAD v4: 6-47710477-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.47710477A>G , CM000668.2:g.47710477A>G GRCh38
NC_000006.11:g.47678213A>G , CM000668.1:g.47678213A>G GRCh37
NC_000006.10:g.47786172A>G NCBI36
NG_052799.1:g.29614A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000283303.3:c.149-258A>G MANE Select ENSP00000283303.2:n.149-258A>G
ENST00000283303.2:c.149-258A>G ENSP00000283303.2:n.149-258A>G
ENST00000327753.7:c.149-258A>G ENSP00000328319.3:n.149-258A>G
ENST00000371220.5:c.320-258A>G ENSP00000360264.1:n.320-258A>G
NM_153838.3:c.149-258A>G NP_722580.3:n.149-258A>G
NM_001347855.1:c.149-258A>G NP_001334784.1:n.149-258A>G
NM_153838.4:c.149-258A>G NP_722580.3:n.149-258A>G
NM_001347855.2:c.149-258A>G NP_001334784.1:n.149-258A>G
NM_153838.5:c.149-258A>G MANE Select NP_722580.3:n.149-258A>G