Canonical Allele Identifier: CA1110104763

Gene:

Linked Data

• dbSNP Id: rs1798577303
• gnomAD v3: 8-5907361-C-T
• gnomAD v4: 8-5907361-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907361C>T , CM000670.2:g.5907361C>T	GRCh38
NC_000008.10:g.5764883C>T , CM000670.1:g.5764883C>T	GRCh37
NC_000008.9:g.5752291C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7630G>A
XR_941375.1:n.308-7630G>A
XR_941376.1:n.406-7630G>A
XR_941377.1:n.308-7630G>A
XR_941378.1:n.216-7630G>A
XR_001745765.1:n.308-7630G>A
XR_001745766.1:n.406-7630G>A
XR_001745767.1:n.216-7630G>A
XR_001745768.1:n.308-7630G>A
XR_941374.2:n.308-7630G>A
XR_941375.2:n.308-7630G>A