Canonical Allele Identifier: CA632130278

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1340599421
• gnomAD v2: 19-16008525-G-C
• gnomAD v3: 19-15897715-G-C
• gnomAD v4: 19-15897715-G-C
• MyVariant Identifiers: chr19:g.16008525G>C (hg19) ; chr19:g.15897715G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897715G>C , CM000681.2:g.15897715G>C	GRCh38
NC_000019.9:g.16008525G>C , CM000681.1:g.16008525G>C	GRCh37
NC_000019.8:g.15869525G>C	NCBI36
NG_007971.2:g.5360C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-103C>G MANE Select	ENSP00000221700.3:n.-1-103C>G
ENST00000011989.11:c.-1-103C>G	ENSP00000011989.8:n.-1-103C>G
ENST00000221700.10:c.-1-103C>G	ENSP00000221700.3:n.-1-103C>G
ENST00000392846.7:n.49+311C>G
ENST00000586927.2:c.-104C>G	ENSP00000465514.1:n.-104C>G
ENST00000587671.2:c.-1-103C>G	ENSP00000467443.2:n.-1-103C>G
ENST00000608168.1:n.53-103C>G
NM_001082.4:c.-1-103C>G	NP_001073.3:n.-1-103C>G
NM_001082.5:c.-1-103C>G MANE Select	NP_001073.3:n.-1-103C>G