Canonical Allele Identifier: CA404579696

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1160682886
• gnomAD v2: 19-16008225-A-G
• gnomAD v4: 19-15897415-A-G
• MyVariant Identifiers: chr19:g.16008225A>G (hg19) ; chr19:g.15897415A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897415A>G , CM000681.2:g.15897415A>G	GRCh38
NC_000019.9:g.16008225A>G , CM000681.1:g.16008225A>G	GRCh37
NC_000019.8:g.15869225A>G	NCBI36
NG_007971.2:g.5660T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.197T>C MANE Select	ENSP00000221700.3:p.Met66Thr
ENST00000011989.11:c.197T>C	ENSP00000011989.8:p.Met66Thr
ENST00000221700.10:c.197T>C	ENSP00000221700.3:p.Met66Thr
ENST00000392846.7:n.49+611T>C
ENST00000586927.2:c.197T>C	ENSP00000465514.1:p.Met66Thr
ENST00000587671.2:c.197T>C	ENSP00000467443.2:p.Met66Thr
ENST00000608168.1:n.250T>C
NM_001082.4:c.197T>C	NP_001073.3:p.Met66Thr
NM_001082.5:c.197T>C MANE Select	NP_001073.3:p.Met66Thr