Canonical Allele Identifier: CA1071983204
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1735983983
gnomAD v3: 4-186191701-G-T
gnomAD v4: 4-186191701-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191701G>T , CM000666.2:g.186191701G>T GRCh38
NC_000004.11:g.187112855G>T , CM000666.1:g.187112855G>T GRCh37
NC_000004.10:g.187349849G>T NCBI36
NG_007965.1:g.5182G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-123G>T MANE Select ENSP00000368079.4:n.-123G>T
ENST00000378802.4:c.-123G>T ENSP00000368079.4:n.-123G>T
NM_207352.3:c.-123G>T NP_997235.3:n.-123G>T
XM_005262935.2:c.-123G>T XP_005262992.1:n.-123G>T
XM_017008037.1:c.-433G>T XP_016863526.1:n.-433G>T
NM_207352.4:c.-123G>T MANE Select NP_997235.3:n.-123G>T
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