Canonical Allele Identifier: CA449667244

Gene: C6orf47 BAG6

Linked Data

• gnomAD v4: 6-31658339-T-C
• MyVariant Identifiers: chr6:g.31626116T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658339T>C , CM000668.2:g.31658339T>C	GRCh38
NC_000006.11:g.31626116T>C , CM000668.1:g.31626116T>C	GRCh37
NC_000006.10:g.31734095T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375911.2:c.*724A>G (C6orf47) MANE Select	ENSP00000365076.1:n.*724A>G
ENST00000375911.1:c.*724A>G (C6orf47)	ENSP00000365076.1:n.*724A>G
NM_021184.3:c.*724A>G (C6orf47)	NP_067007.3:n.*724A>G
XM_011514895.1:c.-14+1982A>G (BAG6)	XP_011513197.1:n.-14+1982A>G
XM_017011279.2:c.-14+1982A>G (BAG6)	XP_016866768.1:n.-14+1982A>G
NM_021184.4:c.*724A>G (C6orf47) MANE Select	NP_067007.3:n.*724A>G