Canonical Allele Identifier: CA1038177471

Gene:

Linked Data

• dbSNP Id: rs1683141243
• gnomAD v3: 2-155870280-T-C
• gnomAD v4: 2-155870280-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870280T>C , CM000664.2:g.155870280T>C	GRCh38
NC_000002.11:g.156726792T>C , CM000664.1:g.156726792T>C	GRCh37
NC_000002.10:g.156435038T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3093A>G
XR_001739749.1:n.331-29296A>G
XR_001739750.1:n.331-29296A>G
XR_001739751.1:n.331-29296A>G
XR_923501.2:n.331-3093A>G