Canonical Allele Identifier: CA65189718
Gene: ERBB4 HGNC NCBI

Linked Data

dbSNP Id: rs839523
gnomAD v2: 2-212816089-C-T
gnomAD v3: 2-211951364-C-T
gnomAD v4: 2-211951364-C-T
MyVariant Identifiers: chr2:g.212816089C>T (hg19) chr2:g.211951364C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211951364C>T , CM000664.2:g.211951364C>T GRCh38
NC_000002.11:g.212816089C>T , CM000664.1:g.212816089C>T GRCh37
NC_000002.10:g.212524334C>T NCBI36
NG_011805.1:g.592264G>A
NG_011805.2:g.592265G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260943.11:c.235-3748G>A ENSP00000260943.7:n.235-3748G>A
ENST00000342788.9:c.235-3748G>A MANE Select ENSP00000342235.4:n.235-3748G>A
ENST00000402597.6:c.157-3748G>A ENSP00000385565.3:n.157-3748G>A
ENST00000260943.10:c.234-3748G>A
ENST00000342788.8:c.235-3748G>A ENSP00000342235.4:n.235-3748G>A
ENST00000402597.5:c.58-3748G>A ENSP00000385565.2:n.58-3748G>A
ENST00000435846.1:c.58-3748G>A ENSP00000405564.1:n.58-3748G>A
ENST00000436443.5:c.235-3748G>A ENSP00000403204.1:n.235-3748G>A
ENST00000484474.1:n.152-3748G>A
ENST00000484594.5:n.287-3748G>A
NM_001042599.1:c.235-3748G>A NP_001036064.1:n.235-3748G>A
NM_005235.2:c.235-3748G>A NP_005226.1:n.235-3748G>A
XM_005246375.1:c.235-3748G>A XP_005246432.1:n.235-3748G>A
XM_005246376.1:c.235-3748G>A XP_005246433.1:n.235-3748G>A
XM_005246377.1:c.235-3748G>A XP_005246434.1:n.235-3748G>A
XM_006712364.1:c.235-3748G>A XP_006712427.1:n.235-3748G>A
XM_005246376.3:c.235-3748G>A XP_005246433.1:n.235-3748G>A
XM_005246377.3:c.235-3748G>A XP_005246434.1:n.235-3748G>A
XM_006712364.3:c.235-3748G>A XP_006712427.1:n.235-3748G>A
XM_017003577.2:c.235-3748G>A XP_016859066.1:n.235-3748G>A
XM_017003578.2:c.235-3748G>A XP_016859067.1:n.235-3748G>A
XM_017003579.2:c.235-3748G>A XP_016859068.1:n.235-3748G>A
XM_017003580.2:c.235-3748G>A XP_016859069.1:n.235-3748G>A
XM_017003581.2:c.235-3748G>A XP_016859070.1:n.235-3748G>A
NM_005235.3:c.235-3748G>A MANE Select NP_005226.1:n.235-3748G>A
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