Canonical Allele Identifier: CA305910158
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs916031211
gnomAD v3: 19-15897785-A-G
gnomAD v4: 19-15897785-A-G
MyVariant Identifiers: chr19:g.16008595A>G (hg19) chr19:g.15897785A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897785A>G , CM000681.2:g.15897785A>G GRCh38
NC_000019.9:g.16008595A>G , CM000681.1:g.16008595A>G GRCh37
NC_000019.8:g.15869595A>G NCBI36
NG_007971.2:g.5290T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-173T>C MANE Select ENSP00000221700.3:n.-1-173T>C
ENST00000011989.11:c.-1-173T>C ENSP00000011989.8:n.-1-173T>C
ENST00000221700.10:c.-1-173T>C ENSP00000221700.3:n.-1-173T>C
ENST00000392846.7:n.49+241T>C
ENST00000587671.2:c.-1-173T>C ENSP00000467443.2:n.-1-173T>C
ENST00000608168.1:n.53-173T>C
NM_001082.4:c.-1-173T>C NP_001073.3:n.-1-173T>C
NM_001082.5:c.-1-173T>C MANE Select NP_001073.3:n.-1-173T>C
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