Canonical Allele Identifier: CA2657649608
Gene:

Linked Data

gnomAD v4: 2-1554179-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554179G>T , CM000664.2:g.1554179G>T GRCh38
NC_000002.11:g.1557951G>T , CM000664.1:g.1557951G>T GRCh37
NC_000002.10:g.1536958G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510447.1:c.-994G>T XP_011508749.1:n.-994G>T
XM_011510448.1:c.-994G>T XP_011508750.1:n.-994G>T
XR_922720.1:n.85+2319C>A
XM_017005455.1:c.-994G>T XP_016860944.1:n.-994G>T
NR_168373.1:n.755G>T