Canonical Allele Identifier: CA772086012

Gene: HCRT

Linked Data

• dbSNP Id: rs1252476330
• gnomAD v3: 17-42184739-G-A
• gnomAD v4: 17-42184739-G-A
• MyVariant Identifiers: chr17:g.40336757G>A (hg19) ; chr17:g.42184739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42184739G>A , CM000679.2:g.42184739G>A	GRCh38
NC_000017.10:g.40336757G>A , CM000679.1:g.40336757G>A	GRCh37
NC_000017.9:g.37590283G>A	NCBI36
NG_011448.1:g.5714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293330.1:c.22-211C>T MANE Select	ENSP00000293330.1:n.22-211C>T
NM_001524.1:c.22-211C>T MANE Select	NP_001515.1:n.22-211C>T