Canonical Allele Identifier: CA792317595
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1303404599
MyVariant Identifiers: chr4:g.187115498_187115499insA (hg19) chr4:g.186194344_186194345insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194345dup , CM000666.2:g.186194345dup GRCh38
NC_000004.11:g.187115499dup , CM000666.1:g.187115499dup GRCh37
NC_000004.10:g.187352493dup NCBI36
NG_007965.1:g.7826dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-155dup MANE Select ENSP00000368079.4:n.215-155dup
ENST00000378802.4:c.215-155dup ENSP00000368079.4:n.215-155dup
NM_207352.3:c.215-155dup NP_997235.3:n.215-155dup
XM_005262935.2:c.215-155dup XP_005262992.1:n.215-155dup
XM_005262935.4:c.215-155dup XP_005262992.1:n.215-155dup
XM_017008037.1:c.-96-155dup XP_016863526.1:n.-96-155dup
NM_207352.4:c.215-155dup MANE Select NP_997235.3:n.215-155dup
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