Canonical Allele Identifier: CA374039261
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1278545974
gnomAD v2: 9-95481665-T-G
gnomAD v3: 9-92719383-T-G
gnomAD v4: 9-92719383-T-G
MyVariant Identifiers: chr9:g.95481665T>G (hg19) chr9:g.92719383T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719383T>G , CM000671.2:g.92719383T>G GRCh38
NC_000009.11:g.95481665T>G , CM000671.1:g.95481665T>G GRCh37
NC_000009.10:g.94521486T>G NCBI36
NG_033908.1:g.50419A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1262A>C MANE Select ENSP00000349351.6:p.Asp421Ala
ENST00000356884.10:c.1262A>C ENSP00000349351.6:p.Asp421Ala
ENST00000375512.3:c.1262A>C ENSP00000364662.3:p.Asp421Ala
NM_001003800.1:c.1262A>C NP_001003800.1:p.Asp421Ala
NM_015250.3:c.1262A>C NP_056065.1:p.Asp421Ala
XM_017014551.1:c.1343A>C XP_016870040.1:p.Asp448Ala
NM_001003800.2:c.1262A>C MANE Select NP_001003800.1:p.Asp421Ala
NM_015250.4:c.1262A>C NP_056065.1:p.Asp421Ala
Search 100 bp 5'
Search 100 bp 3'