Canonical Allele Identifier: CA112120731
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs917834474
gnomAD v2: 4-187115315-A-T
gnomAD v3: 4-186194161-A-T
gnomAD v4: 4-186194161-A-T
MyVariant Identifiers: chr4:g.187115315A>T (hg19) chr4:g.186194161A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194161A>T , CM000666.2:g.186194161A>T GRCh38
NC_000004.11:g.187115315A>T , CM000666.1:g.187115315A>T GRCh37
NC_000004.10:g.187352309A>T NCBI36
NG_007965.1:g.7642A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-339A>T MANE Select ENSP00000368079.4:n.215-339A>T
ENST00000378802.4:c.215-339A>T ENSP00000368079.4:n.215-339A>T
NM_207352.3:c.215-339A>T NP_997235.3:n.215-339A>T
XM_005262935.2:c.215-339A>T XP_005262992.1:n.215-339A>T
XM_005262935.4:c.215-339A>T XP_005262992.1:n.215-339A>T
XM_017008037.1:c.-96-339A>T XP_016863526.1:n.-96-339A>T
NM_207352.4:c.215-339A>T MANE Select NP_997235.3:n.215-339A>T
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