Canonical Allele Identifier: CA358946829
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115669T>C (hg19) chr4:g.186194515T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194515T>C , CM000666.2:g.186194515T>C GRCh38
NC_000004.11:g.187115669T>C , CM000666.1:g.187115669T>C GRCh37
NC_000004.10:g.187352663T>C NCBI36
NG_007965.1:g.7996T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.230T>C MANE Select ENSP00000368079.4:p.Ile77Thr
ENST00000378802.4:c.230T>C ENSP00000368079.4:p.Ile77Thr
NM_207352.3:c.230T>C NP_997235.3:p.Ile77Thr
XM_005262935.2:c.230T>C XP_005262992.1:p.Ile77Thr
XM_005262935.4:c.230T>C XP_005262992.1:p.Ile77Thr
XM_017008037.1:c.-81T>C XP_016863526.1:n.-81T>C
NM_207352.4:c.230T>C MANE Select NP_997235.3:p.Ile77Thr
Search 100 bp 5'
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