Canonical Allele Identifier: CA149263617

Gene:

Linked Data

• dbSNP Id: rs922461382
• gnomAD v3: 6-140848715-T-C
• gnomAD v4: 6-140848715-T-C
• MyVariant Identifiers: chr6:g.141169852T>C (hg19) ; chr6:g.140848715T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.140848715T>C , CM000668.2:g.140848715T>C	GRCh38
NC_000006.11:g.141169852T>C , CM000668.1:g.141169852T>C	GRCh37
NC_000006.10:g.141211545T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_428030.2:n.327-2411A>G
XR_943075.1:n.315-2411A>G
XR_943076.1:n.246-2411A>G
XR_001744390.1:n.235-32485A>G
XR_428030.4:n.341-2411A>G
XR_943075.3:n.329-2411A>G