Canonical Allele Identifier: CA374034039
Gene: BICD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718592T>A , CM000671.2:g.92718592T>A GRCh38
NC_000009.11:g.95480874T>A , CM000671.1:g.95480874T>A GRCh37
NC_000009.10:g.94520695T>A NCBI36
NG_033908.1:g.51210A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2053A>T MANE Select ENSP00000349351.6:p.Thr685Ser
ENST00000356884.10:c.2053A>T ENSP00000349351.6:p.Thr685Ser
ENST00000375512.3:c.2053A>T ENSP00000364662.3:p.Thr685Ser
NM_001003800.1:c.2053A>T NP_001003800.1:p.Thr685Ser
NM_015250.3:c.2053A>T NP_056065.1:p.Thr685Ser
XM_017014551.1:c.2134A>T XP_016870040.1:p.Thr712Ser
NM_001003800.2:c.2053A>T MANE Select NP_001003800.1:p.Thr685Ser
NM_015250.4:c.2053A>T NP_056065.1:p.Thr685Ser