Canonical Allele Identifier: CA374040167
Gene: BICD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719474T>A , CM000671.2:g.92719474T>A GRCh38
NC_000009.11:g.95481756T>A , CM000671.1:g.95481756T>A GRCh37
NC_000009.10:g.94521577T>A NCBI36
NG_033908.1:g.50328A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1171A>T MANE Select ENSP00000349351.6:p.Thr391Ser
ENST00000356884.10:c.1171A>T ENSP00000349351.6:p.Thr391Ser
ENST00000375512.3:c.1171A>T ENSP00000364662.3:p.Thr391Ser
NM_001003800.1:c.1171A>T NP_001003800.1:p.Thr391Ser
NM_015250.3:c.1171A>T NP_056065.1:p.Thr391Ser
XM_017014551.1:c.1252A>T XP_016870040.1:p.Thr418Ser
NM_001003800.2:c.1171A>T MANE Select NP_001003800.1:p.Thr391Ser
NM_015250.4:c.1171A>T NP_056065.1:p.Thr391Ser