Canonical Allele Identifier: CA783707153
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1270006547
MyVariant Identifiers: chr19:g.15989976C>G (hg19) chr19:g.15879166C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879166C>G , CM000681.2:g.15879166C>G GRCh38
NC_000019.9:g.15989976C>G , CM000681.1:g.15989976C>G GRCh37
NC_000019.8:g.15850976C>G NCBI36
NG_007971.2:g.23909G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+180G>C MANE Select ENSP00000221700.3:n.1397+180G>C
ENST00000011989.11:c.1397+180G>C ENSP00000011989.8:n.1397+180G>C
ENST00000221700.10:c.1397+180G>C ENSP00000221700.3:n.1397+180G>C
ENST00000392846.7:n.1340+180G>C
ENST00000589654.2:c.185+180G>C
NM_001082.4:c.1397+180G>C NP_001073.3:n.1397+180G>C
NM_001082.5:c.1397+180G>C MANE Select NP_001073.3:n.1397+180G>C
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