Canonical Allele Identifier: CA819569641

Gene:

Linked Data

• dbSNP Id: rs1297871232
• gnomAD v3: 6-137416260-G-T
• gnomAD v4: 6-137416260-G-T
• MyVariant Identifiers: chr6:g.137737397G>T (hg19) ; chr6:g.137416260G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137416260G>T , CM000668.2:g.137416260G>T	GRCh38
NC_000006.11:g.137737397G>T , CM000668.1:g.137737397G>T	GRCh37
NC_000006.10:g.137779090G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943047.1:n.798+362G>T
XR_943053.1:n.798+362G>T
XR_943055.1:n.798+362G>T