Canonical Allele Identifier: CA2672891888
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191713-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191713G>T , CM000666.2:g.186191713G>T GRCh38
NC_000004.11:g.187112867G>T , CM000666.1:g.187112867G>T GRCh37
NC_000004.10:g.187349861G>T NCBI36
NG_007965.1:g.5194G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-111G>T MANE Select ENSP00000368079.4:n.-111G>T
ENST00000378802.4:c.-111G>T ENSP00000368079.4:n.-111G>T
NM_207352.3:c.-111G>T NP_997235.3:n.-111G>T
XM_005262935.2:c.-111G>T XP_005262992.1:n.-111G>T
XM_017008037.1:c.-421G>T XP_016863526.1:n.-421G>T
NM_207352.4:c.-111G>T MANE Select NP_997235.3:n.-111G>T
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