Canonical Allele Identifier: CA9269784
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs764224671
ExAC: 19:15651580 G / T
gnomAD v4: 19-15540769-G-T
MyVariant Identifiers: chr19:g.15651580G>T (hg19) chr19:g.15540769G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540769G>T , CM000681.2:g.15540769G>T GRCh38
NC_000019.9:g.15651580G>T , CM000681.1:g.15651580G>T GRCh37
NC_000019.8:g.15512580G>T NCBI36
NG_007987.1:g.37245G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+52G>T MANE Select ENSP00000269703.1:n.939+52G>T
ENST00000269703.7:c.939+52G>T ENSP00000269703.1:n.939+52G>T
ENST00000601005.2:c.939+52G>T ENSP00000469866.1:n.939+52G>T
NM_173483.3:c.939+52G>T NP_775754.2:n.939+52G>T
XM_011527692.1:c.939+52G>T XP_011525994.1:n.939+52G>T
XM_011527693.1:c.939+52G>T XP_011525995.1:n.939+52G>T
XM_011527692.2:c.939+52G>T XP_011525994.1:n.939+52G>T
XM_011527693.2:c.939+52G>T XP_011525995.1:n.939+52G>T
NM_173483.4:c.939+52G>T MANE Select NP_775754.2:n.939+52G>T
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