Canonical Allele Identifier: CA9273673

Gene: CYP4F2

Linked Data

• dbSNP Id: rs781012436
• ExAC: 19:15990375 G / A
• gnomAD v2: 19-15990375-G-A
• gnomAD v4: 19-15879565-G-A
• MyVariant Identifiers: chr19:g.15990375G>A (hg19) ; chr19:g.15879565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879565G>A , CM000681.2:g.15879565G>A	GRCh38
NC_000019.9:g.15990375G>A , CM000681.1:g.15990375G>A	GRCh37
NC_000019.8:g.15851375G>A	NCBI36
NG_007971.2:g.23510C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1314+39C>T MANE Select	ENSP00000221700.3:n.1314+39C>T
ENST00000011989.11:c.1314+39C>T	ENSP00000011989.8:n.1314+39C>T
ENST00000221700.10:c.1314+39C>T	ENSP00000221700.3:n.1314+39C>T
ENST00000392846.7:n.1257+39C>T
ENST00000589654.2:c.103-137C>T
NM_001082.4:c.1314+39C>T	NP_001073.3:n.1314+39C>T
NM_001082.5:c.1314+39C>T MANE Select	NP_001073.3:n.1314+39C>T