Canonical Allele Identifier: CA9269740
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs754519171
ExAC: 19:15651540 CCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG / C
gnomAD v2: 19-15651540-CCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG-C
gnomAD v4: 19-15540729-CCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG-C
MyVariant Identifiers: chr19:g.15651541_15651586del (hg19) chr19:g.15540730_15540775del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540731_15540776del , CM000681.2:g.15540731_15540776del GRCh38
NC_000019.9:g.15651542_15651587del , CM000681.1:g.15651542_15651587del GRCh37
NC_000019.8:g.15512542_15512587del NCBI36
NG_007987.1:g.37207_37252del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+14_939+59del MANE Select ENSP00000269703.1:n.939+14_939+59del
ENST00000269703.7:c.939+14_939+59del ENSP00000269703.1:n.939+14_939+59del
ENST00000601005.2:c.939+14_939+59del ENSP00000469866.1:n.939+14_939+59del
NM_173483.3:c.939+14_939+59del NP_775754.2:n.939+14_939+59del
XM_011527692.1:c.939+14_939+59del XP_011525994.1:n.939+14_939+59del
XM_011527693.1:c.939+14_939+59del XP_011525995.1:n.939+14_939+59del
XM_011527692.2:c.939+14_939+59del XP_011525994.1:n.939+14_939+59del
XM_011527693.2:c.939+14_939+59del XP_011525995.1:n.939+14_939+59del
NM_173483.4:c.939+14_939+59del MANE Select NP_775754.2:n.939+14_939+59del
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