Canonical Allele Identifier: CA466343014
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481109G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718827G>A , CM000671.2:g.92718827G>A GRCh38
NC_000009.11:g.95481109G>A , CM000671.1:g.95481109G>A GRCh37
NC_000009.10:g.94520930G>A NCBI36
NG_033908.1:g.50975C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1818C>T MANE Select ENSP00000349351.6:p.Ser606=
ENST00000356884.10:c.1818C>T ENSP00000349351.6:p.Ser606=
ENST00000375512.3:c.1818C>T ENSP00000364662.3:p.Ser606=
NM_001003800.1:c.1818C>T NP_001003800.1:p.Ser606=
NM_015250.3:c.1818C>T NP_056065.1:p.Ser606=
XM_017014551.1:c.1899C>T XP_016870040.1:p.Ser633=
NM_001003800.2:c.1818C>T MANE Select NP_001003800.1:p.Ser606=
NM_015250.4:c.1818C>T NP_056065.1:p.Ser606=
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