Canonical Allele Identifier: CA449667306
Gene: C6orf47 HGNC NCBI
BAG6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31626137T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658360T>G , CM000668.2:g.31658360T>G GRCh38
NC_000006.11:g.31626137T>G , CM000668.1:g.31626137T>G GRCh37
NC_000006.10:g.31734116T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375911.2:c.*703A>C (C6orf47) MANE Select ENSP00000365076.1:n.*703A>C
ENST00000375911.1:c.*703A>C (C6orf47) ENSP00000365076.1:n.*703A>C
NM_021184.3:c.*703A>C (C6orf47) NP_067007.3:n.*703A>C
XM_011514895.1:c.-14+1961A>C (BAG6) XP_011513197.1:n.-14+1961A>C
XM_017011279.2:c.-14+1961A>C (BAG6) XP_016866768.1:n.-14+1961A>C
NM_021184.4:c.*703A>C (C6orf47) MANE Select NP_067007.3:n.*703A>C