Canonical Allele Identifier: CA466343154
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481265C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718983C>A , CM000671.2:g.92718983C>A GRCh38
NC_000009.11:g.95481265C>A , CM000671.1:g.95481265C>A GRCh37
NC_000009.10:g.94521086C>A NCBI36
NG_033908.1:g.50819G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1662G>T MANE Select ENSP00000349351.6:p.Leu554=
ENST00000356884.10:c.1662G>T ENSP00000349351.6:p.Leu554=
ENST00000375512.3:c.1662G>T ENSP00000364662.3:p.Leu554=
NM_001003800.1:c.1662G>T NP_001003800.1:p.Leu554=
NM_015250.3:c.1662G>T NP_056065.1:p.Leu554=
XM_017014551.1:c.1743G>T XP_016870040.1:p.Leu581=
NM_001003800.2:c.1662G>T MANE Select NP_001003800.1:p.Leu554=
NM_015250.4:c.1662G>T NP_056065.1:p.Leu554=
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