Canonical Allele Identifier: CA632129616
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs752456781
gnomAD v2: 19-15651578-G-T
gnomAD v4: 19-15540767-G-T
MyVariant Identifiers: chr19:g.15651578G>T (hg19) chr19:g.15540767G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540767G>T , CM000681.2:g.15540767G>T GRCh38
NC_000019.9:g.15651578G>T , CM000681.1:g.15651578G>T GRCh37
NC_000019.8:g.15512578G>T NCBI36
NG_007987.1:g.37243G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+50G>T MANE Select ENSP00000269703.1:n.939+50G>T
ENST00000269703.7:c.939+50G>T ENSP00000269703.1:n.939+50G>T
ENST00000601005.2:c.939+50G>T ENSP00000469866.1:n.939+50G>T
NM_173483.3:c.939+50G>T NP_775754.2:n.939+50G>T
XM_011527692.1:c.939+50G>T XP_011525994.1:n.939+50G>T
XM_011527693.1:c.939+50G>T XP_011525995.1:n.939+50G>T
XM_011527692.2:c.939+50G>T XP_011525994.1:n.939+50G>T
XM_011527693.2:c.939+50G>T XP_011525995.1:n.939+50G>T
NM_173483.4:c.939+50G>T MANE Select NP_775754.2:n.939+50G>T
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