Canonical Allele Identifier: CA374034096
Gene: BICD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718598G>A , CM000671.2:g.92718598G>A GRCh38
NC_000009.11:g.95480880G>A , CM000671.1:g.95480880G>A GRCh37
NC_000009.10:g.94520701G>A NCBI36
NG_033908.1:g.51204C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2047C>T MANE Select ENSP00000349351.6:p.Leu683Phe
ENST00000356884.10:c.2047C>T ENSP00000349351.6:p.Leu683Phe
ENST00000375512.3:c.2047C>T ENSP00000364662.3:p.Leu683Phe
NM_001003800.1:c.2047C>T NP_001003800.1:p.Leu683Phe
NM_015250.3:c.2047C>T NP_056065.1:p.Leu683Phe
XM_017014551.1:c.2128C>T XP_016870040.1:p.Leu710Phe
NM_001003800.2:c.2047C>T MANE Select NP_001003800.1:p.Leu683Phe
NM_015250.4:c.2047C>T NP_056065.1:p.Leu683Phe