Canonical Allele Identifier: CA2576657766
Gene: CYP4F22 HGNC NCBI

Linked Data

gnomAD v4: 19-15529626-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529626G>C , CM000681.2:g.15529626G>C GRCh38
NC_000019.9:g.15640437G>C , CM000681.1:g.15640437G>C GRCh37
NC_000019.8:g.15501437G>C NCBI36
NG_007987.1:g.26102G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.223-83G>C MANE Select ENSP00000269703.1:n.223-83G>C
ENST00000269703.7:c.223-83G>C ENSP00000269703.1:n.223-83G>C
ENST00000601005.2:c.223-83G>C ENSP00000469866.1:n.223-83G>C
NM_173483.3:c.223-83G>C NP_775754.2:n.223-83G>C
XM_011527692.1:c.223-83G>C XP_011525994.1:n.223-83G>C
XM_011527693.1:c.223-83G>C XP_011525995.1:n.223-83G>C
XM_011527692.2:c.223-83G>C XP_011525994.1:n.223-83G>C
XM_011527693.2:c.223-83G>C XP_011525995.1:n.223-83G>C
NM_173483.4:c.223-83G>C MANE Select NP_775754.2:n.223-83G>C
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