Canonical Allele Identifier: CA374038937
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481612A>C (hg19) chr9:g.92719330A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719330A>C , CM000671.2:g.92719330A>C GRCh38
NC_000009.11:g.95481612A>C , CM000671.1:g.95481612A>C GRCh37
NC_000009.10:g.94521433A>C NCBI36
NG_033908.1:g.50472T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1315T>G MANE Select ENSP00000349351.6:p.Tyr439Asp
ENST00000356884.10:c.1315T>G ENSP00000349351.6:p.Tyr439Asp
ENST00000375512.3:c.1315T>G ENSP00000364662.3:p.Tyr439Asp
NM_001003800.1:c.1315T>G NP_001003800.1:p.Tyr439Asp
NM_015250.3:c.1315T>G NP_056065.1:p.Tyr439Asp
XM_017014551.1:c.1396T>G XP_016870040.1:p.Tyr466Asp
NM_001003800.2:c.1315T>G MANE Select NP_001003800.1:p.Tyr439Asp
NM_015250.4:c.1315T>G NP_056065.1:p.Tyr439Asp
Search 100 bp 5'
Search 100 bp 3'