Canonical Allele Identifier: CA466343156
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1190861854
gnomAD v2: 9-95481265-C-T
gnomAD v4: 9-92718983-C-T

Genomic Alleles

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

Transcript Alleles

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