Canonical Allele Identifier: CA12363641

Gene: TXLNB

Linked Data

• dbSNP Id: rs12660752
• gnomAD v2: 6-139518710-G-A
• gnomAD v3: 6-139197573-G-A
• gnomAD v4: 6-139197573-G-A
• MyVariant Identifiers: chr6:g.139518710G>A (hg19) ; chr6:g.139197573G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139197573G>A , CM000668.2:g.139197573G>A	GRCh38
NC_000006.11:g.139518710G>A , CM000668.1:g.139518710G>A	GRCh37
NC_000006.10:g.139560403G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942314.1:n.1625-27009C>T
XR_942315.1:n.1794+4102C>T
XR_942316.1:n.1733+4102C>T
XR_942317.1:n.1625-27009C>T
XR_942317.3:n.1682-27009C>T