Canonical Allele Identifier: CA374038347
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481525C>A (hg19) chr9:g.92719243C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719243C>A , CM000671.2:g.92719243C>A GRCh38
NC_000009.11:g.95481525C>A , CM000671.1:g.95481525C>A GRCh37
NC_000009.10:g.94521346C>A NCBI36
NG_033908.1:g.50559G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1402G>T MANE Select ENSP00000349351.6:p.Ala468Ser
ENST00000356884.10:c.1402G>T ENSP00000349351.6:p.Ala468Ser
ENST00000375512.3:c.1402G>T ENSP00000364662.3:p.Ala468Ser
NM_001003800.1:c.1402G>T NP_001003800.1:p.Ala468Ser
NM_015250.3:c.1402G>T NP_056065.1:p.Ala468Ser
XM_017014551.1:c.1483G>T XP_016870040.1:p.Ala495Ser
NM_001003800.2:c.1402G>T MANE Select NP_001003800.1:p.Ala468Ser
NM_015250.4:c.1402G>T NP_056065.1:p.Ala468Ser
Search 100 bp 5'
Search 100 bp 3'