Canonical Allele Identifier: CA557395891
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1486120621
gnomAD v2: 4-187112957-C-T
gnomAD v4: 4-186191803-C-T
MyVariant Identifiers: chr4:g.187112957C>T (hg19) chr4:g.186191803C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191803C>T , CM000666.2:g.186191803C>T GRCh38
NC_000004.11:g.187112957C>T , CM000666.1:g.187112957C>T GRCh37
NC_000004.10:g.187349951C>T NCBI36
NG_007965.1:g.5284C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-21C>T MANE Select ENSP00000368079.4:n.-21C>T
ENST00000378802.4:c.-21C>T ENSP00000368079.4:n.-21C>T
NM_207352.3:c.-21C>T NP_997235.3:n.-21C>T
XM_005262935.2:c.-21C>T XP_005262992.1:n.-21C>T
XM_005262935.4:c.-21C>T XP_005262992.1:n.-21C>T
XM_017008037.1:c.-331C>T XP_016863526.1:n.-331C>T
NM_207352.4:c.-21C>T MANE Select NP_997235.3:n.-21C>T
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