Canonical Allele Identifier: CA374034872
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1230428645
gnomAD v2: 9-95481000-C-T
gnomAD v3: 9-92718718-C-T
gnomAD v4: 9-92718718-C-T
MyVariant Identifiers: chr9:g.95481000C>T (hg19) chr9:g.92718718C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718718C>T , CM000671.2:g.92718718C>T GRCh38
NC_000009.11:g.95481000C>T , CM000671.1:g.95481000C>T GRCh37
NC_000009.10:g.94520821C>T NCBI36
NG_033908.1:g.51084G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1927G>A MANE Select ENSP00000349351.6:p.Ala643Thr
ENST00000356884.10:c.1927G>A ENSP00000349351.6:p.Ala643Thr
ENST00000375512.3:c.1927G>A ENSP00000364662.3:p.Ala643Thr
NM_001003800.1:c.1927G>A NP_001003800.1:p.Ala643Thr
NM_015250.3:c.1927G>A NP_056065.1:p.Ala643Thr
XM_017014551.1:c.2008G>A XP_016870040.1:p.Ala670Thr
NM_001003800.2:c.1927G>A MANE Select NP_001003800.1:p.Ala643Thr
NM_015250.4:c.1927G>A NP_056065.1:p.Ala643Thr
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