Canonical Allele Identifier: CA837502821
Gene: CRHR2 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30669859C>G , CM000669.2:g.30669859C>G GRCh38
NC_000007.13:g.30709475C>G , CM000669.1:g.30709475C>G GRCh37
NC_000007.12:g.30676000C>G NCBI36
NG_029169.1:g.35245G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471646.6:c.230-2546G>C MANE Select ENSP00000418722.1:n.230-2546G>C
ENST00000341843.8:c.188-2546G>C ENSP00000344304.4:n.188-2546G>C
ENST00000348438.8:c.311-2546G>C ENSP00000340943.4:n.311-2546G>C
ENST00000452278.5:c.*343-2546G>C ENSP00000401930.1:n.*343-2546G>C
ENST00000471646.5:c.230-2546G>C ENSP00000418722.1:n.230-2546G>C
ENST00000506074.6:c.230-2546G>C ENSP00000426498.3:n.230-2546G>C
NM_001202475.1:c.311-2546G>C NP_001189404.1:n.311-2546G>C
NM_001202481.1:c.188-2546G>C NP_001189410.1:n.188-2546G>C
NM_001202482.1:c.230-2546G>C NP_001189411.1:n.230-2546G>C
NM_001202483.1:c.230-2546G>C NP_001189412.1:n.230-2546G>C
NM_001883.4:c.230-2546G>C NP_001874.2:n.230-2546G>C
XM_011515127.1:c.230-2546G>C XP_011513429.1:n.230-2546G>C
XM_011515128.1:c.230-2546G>C XP_011513430.1:n.230-2546G>C
XM_011515129.1:c.230-2546G>C XP_011513431.1:n.230-2546G>C
XM_017011752.2:c.188-2546G>C XP_016867241.1:n.188-2546G>C
XM_024446665.1:c.230-2546G>C XP_024302433.1:n.230-2546G>C
NM_001883.5:c.230-2546G>C MANE Select NP_001874.2:n.230-2546G>C
NM_001202482.2:c.230-2546G>C NP_001189411.1:n.230-2546G>C
NM_001202483.2:c.230-2546G>C NP_001189412.1:n.230-2546G>C