Canonical Allele Identifier: CA829017279

Gene:

Linked Data

• dbSNP Id: rs1455687139
• gnomAD v3: 6-8525231-T-TATA
• gnomAD v4: 6-8525231-T-TATA
• MyVariant Identifiers: chr6:g.8525464_8525465insATA (hg19) ; chr6:g.8525231_8525232insATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8525232_8525234dup , CM000668.2:g.8525232_8525234dup	GRCh38
NC_000006.11:g.8525465_8525467dup , CM000668.1:g.8525465_8525467dup	GRCh37
NC_000006.10:g.8470464_8470466dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038979.1:n.626-33353_626-33351dup
NR_038980.1:n.649-33353_649-33351dup