Canonical Allele Identifier: CA137969599

Gene: ADGRF4

Linked Data

• dbSNP Id: rs891794138
• gnomAD v2: 6-47678232-T-C
• gnomAD v3: 6-47710496-T-C
• gnomAD v4: 6-47710496-T-C
• MyVariant Identifiers: chr6:g.47678232T>C (hg19) ; chr6:g.47710496T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.47710496T>C , CM000668.2:g.47710496T>C	GRCh38
NC_000006.11:g.47678232T>C , CM000668.1:g.47678232T>C	GRCh37
NC_000006.10:g.47786191T>C	NCBI36
NG_052799.1:g.29633T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283303.3:c.149-239T>C MANE Select	ENSP00000283303.2:n.149-239T>C
ENST00000283303.2:c.149-239T>C	ENSP00000283303.2:n.149-239T>C
ENST00000327753.7:c.149-239T>C	ENSP00000328319.3:n.149-239T>C
ENST00000371220.5:c.320-239T>C	ENSP00000360264.1:n.320-239T>C
NM_153838.3:c.149-239T>C	NP_722580.3:n.149-239T>C
NM_001347855.1:c.149-239T>C	NP_001334784.1:n.149-239T>C
NM_153838.4:c.149-239T>C	NP_722580.3:n.149-239T>C
NM_001347855.2:c.149-239T>C	NP_001334784.1:n.149-239T>C
NM_153838.5:c.149-239T>C MANE Select	NP_722580.3:n.149-239T>C