Canonical Allele Identifier: CA374035613
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481113C>G (hg19) chr9:g.92718831C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718831C>G , CM000671.2:g.92718831C>G GRCh38
NC_000009.11:g.95481113C>G , CM000671.1:g.95481113C>G GRCh37
NC_000009.10:g.94520934C>G NCBI36
NG_033908.1:g.50971G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1814G>C MANE Select ENSP00000349351.6:p.Ser605Thr
ENST00000356884.10:c.1814G>C ENSP00000349351.6:p.Ser605Thr
ENST00000375512.3:c.1814G>C ENSP00000364662.3:p.Ser605Thr
NM_001003800.1:c.1814G>C NP_001003800.1:p.Ser605Thr
NM_015250.3:c.1814G>C NP_056065.1:p.Ser605Thr
XM_017014551.1:c.1895G>C XP_016870040.1:p.Ser632Thr
NM_001003800.2:c.1814G>C MANE Select NP_001003800.1:p.Ser605Thr
NM_015250.4:c.1814G>C NP_056065.1:p.Ser605Thr
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