Canonical Allele Identifier: CA566364392
Gene: BAG6 HGNC NCBI

Linked Data

dbSNP Id: rs1447140883
gnomAD v2: 6-31626025-T-C
gnomAD v3: 6-31658248-T-C
gnomAD v4: 6-31658248-T-C
MyVariant Identifiers: chr6:g.31626025T>C (hg19) chr6:g.31658248T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658248T>C , CM000668.2:g.31658248T>C GRCh38
NC_000006.11:g.31626025T>C , CM000668.1:g.31626025T>C GRCh37
NC_000006.10:g.31734004T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514895.1:c.-14+2073A>G XP_011513197.1:n.-14+2073A>G
XM_017011279.2:c.-14+2073A>G XP_016866768.1:n.-14+2073A>G
Search 100 bp 5'
Search 100 bp 3'