Canonical Allele Identifier: CA566942680

Gene: ADGRF4

Linked Data

• dbSNP Id: rs937888864
• gnomAD v2: 6-47678213-A-T
• gnomAD v3: 6-47710477-A-T
• gnomAD v4: 6-47710477-A-T
• MyVariant Identifiers: chr6:g.47678213A>T (hg19) ; chr6:g.47710477A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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