Canonical Allele Identifier: CA442638736
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115748T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194594T>C , CM000666.2:g.186194594T>C GRCh38
NC_000004.11:g.187115748T>C , CM000666.1:g.187115748T>C GRCh37
NC_000004.10:g.187352742T>C NCBI36
NG_007965.1:g.8075T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.309T>C MANE Select ENSP00000368079.4:p.Tyr103=
ENST00000378802.4:c.309T>C ENSP00000368079.4:p.Tyr103=
NM_207352.3:c.309T>C NP_997235.3:p.Tyr103=
XM_005262935.2:c.309T>C XP_005262992.1:p.Tyr103=
XM_006714184.2:c.-2T>C XP_006714247.1:n.-2T>C
XM_005262935.4:c.309T>C XP_005262992.1:p.Tyr103=
XM_017008037.1:c.-2T>C XP_016863526.1:n.-2T>C
NM_207352.4:c.309T>C MANE Select NP_997235.3:p.Tyr103=
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