Canonical Allele Identifier: CA2670937831

Gene: ALB

Linked Data

• gnomAD v4: 4-73413280-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413280C>T , CM000666.2:g.73413280C>T	GRCh38
NC_000004.11:g.74278997C>T , CM000666.1:g.74278997C>T	GRCh37
NC_000004.10:g.74497861C>T	NCBI36
NG_009291.1:g.14026C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-140C>T MANE Select	ENSP00000295897.4:n.844-140C>T
ENST00000295897.8:c.844-140C>T	ENSP00000295897.4:n.844-140C>T
ENST00000401494.7:c.499-140C>T	ENSP00000384695.3:n.499-140C>T
ENST00000415165.6:c.268-140C>T	ENSP00000401820.2:n.268-140C>T
ENST00000476441.6:c.*123-140C>T	ENSP00000423727.1:n.*123-140C>T
ENST00000484992.1:n.24C>T
ENST00000503124.5:c.394-140C>T	ENSP00000421027.1:n.394-140C>T
ENST00000505649.5:n.530-140C>T
ENST00000509063.5:c.844-140C>T	ENSP00000422784.1:n.844-140C>T
ENST00000511370.1:c.377-140C>T
ENST00000621085.4:c.491-1826C>T	ENSP00000483421.1:n.491-1826C>T
ENST00000621628.4:c.487-1822C>T	ENSP00000480485.1:n.487-1822C>T
NM_000477.5:c.844-140C>T	NP_000468.1:n.844-140C>T
NM_000477.6:c.844-140C>T	NP_000468.1:n.844-140C>T
NM_000477.7:c.844-140C>T MANE Select	NP_000468.1:n.844-140C>T