Canonical Allele Identifier: CA9269671
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs764984151
ExAC: 19:15651255 T / C
gnomAD v2: 19-15651255-T-C
gnomAD v3: 19-15540444-T-C
gnomAD v4: 19-15540444-T-C
MyVariant Identifiers: chr19:g.15651255T>C (hg19) chr19:g.15540444T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540444T>C , CM000681.2:g.15540444T>C GRCh38
NC_000019.9:g.15651255T>C , CM000681.1:g.15651255T>C GRCh37
NC_000019.8:g.15512255T>C NCBI36
NG_007987.1:g.36920T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.672-6T>C MANE Select ENSP00000269703.1:n.672-6T>C
ENST00000269703.7:c.672-6T>C ENSP00000269703.1:n.672-6T>C
ENST00000601005.2:c.672-6T>C ENSP00000469866.1:n.672-6T>C
NM_173483.3:c.672-6T>C NP_775754.2:n.672-6T>C
XM_011527692.1:c.672-6T>C XP_011525994.1:n.672-6T>C
XM_011527693.1:c.672-6T>C XP_011525995.1:n.672-6T>C
XM_011527692.2:c.672-6T>C XP_011525994.1:n.672-6T>C
XM_011527693.2:c.672-6T>C XP_011525995.1:n.672-6T>C
NM_173483.4:c.672-6T>C MANE Select NP_775754.2:n.672-6T>C
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