Canonical Allele Identifier: CA374038994
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481623A>T (hg19) chr9:g.92719341A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719341A>T , CM000671.2:g.92719341A>T GRCh38
NC_000009.11:g.95481623A>T , CM000671.1:g.95481623A>T GRCh37
NC_000009.10:g.94521444A>T NCBI36
NG_033908.1:g.50461T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1304T>A MANE Select ENSP00000349351.6:p.Leu435Ter
ENST00000356884.10:c.1304T>A ENSP00000349351.6:p.Leu435Ter
ENST00000375512.3:c.1304T>A ENSP00000364662.3:p.Leu435Ter
NM_001003800.1:c.1304T>A NP_001003800.1:p.Leu435Ter
NM_015250.3:c.1304T>A NP_056065.1:p.Leu435Ter
XM_017014551.1:c.1385T>A XP_016870040.1:p.Leu462Ter
NM_001003800.2:c.1304T>A MANE Select NP_001003800.1:p.Leu435Ter
NM_015250.4:c.1304T>A NP_056065.1:p.Leu435Ter
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